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          • Home
          • › Search Tool
          • › Search Results
          • › Hs03787829_cn
          See other KCNQ1-AS1 CNV Assays ›
          Gene Symbol
          KCNQ1-AS1
          Assay Reference Genome
          Location

          Chr.11:2860560 on build GRCh38
          Cytoband
          11p15.4
          Assay ID Hs03787829_cn
          Size
          Availability Made To Order
          Catalog # 4400291
          Price
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          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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          Assay Details

          Target Gene Details

          Entrez Gene ID:

          338653

          Gene Name:

          KCNQ1 antisense RNA 1

          Gene Aliases:

          -

          Location:

          Chr.11:2840135-2861569 on Build GRCh38

          Assay Gene Location:

          Within Intron 1
          Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
          KCNQ1-AS1 NR_130721.1
          AJ251642.1

          Target Copy Number Variation Details

          DGV Version:

          Release date: 2016-05-15, GRCh GRCh38
          Target
          Variation
          Location CNV
          Subtype
          Genes
          esv2759795 Chr.11:2767814 - 2942382 on Build GRCh38 Gain SLC22A18 KCNQ1DN CDKN1C KCNQ1 KCNQ1-AS1 SLC22A18AS PHLDA2
          nsv951292 Chr.11:2792271 - 2927870 on Build GRCh38 Deletion SLC22A18 KCNQ1DN CDKN1C KCNQ1 KCNQ1-AS1 SLC22A18AS
          nsv825715 Chr.11:2855771 - 2890367 on Build GRCh38 Gain KCNQ1DN CDKN1C KCNQ1-AS1 SLC22A18AS
          nsv469930 Chr.11:2831299 - 2924715 on Build GRCh38 Loss SLC22A18 KCNQ1DN CDKN1C KCNQ1 KCNQ1-AS1 SLC22A18AS
          nsv1053066 Chr.11:2829552 - 2872696 on Build GRCh38 Gain KCNQ1DN KCNQ1 KCNQ1-AS1
          nsv553111 Chr.11:2842057 - 2904391 on Build GRCh38 Loss SLC22A18 KCNQ1DN CDKN1C KCNQ1 KCNQ1-AS1 SLC22A18AS
          dgv1574n54 Chr.11:2848935 - 2889391 on Build GRCh38 Loss KCNQ1DN CDKN1C KCNQ1 KCNQ1-AS1 SLC22A18AS

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          More Information


          Set Membership:

          Intragenic Intronic Non-exonic DGV Variation

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