Product Details

Assay Reference Genome
Location

Chr.X:14839507 on build GRCh38
Cytoband
Xp22.2
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs145109079] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Target Gene Details

Entrez Gene ID
2187
Gene Symbol
FANCB
Gene Name
Fanconi anemia complementation group B
Gene Aliases
FA2, FAAP90, FAAP95, FAB, FACB
Location
Chr.X:14690863-14873255 on build GRCh38
Assay Gene Location
Within Intron 11
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
FANCB XM_011545470.2 XP_011543772.1
XM_017029356.1 XP_016884845.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv6812 ChrX:14836320 - 14868456 on Build GRCh38 Deletion FANCB
nsv9934 ChrX:14730738 - 15173654 on Build GRCh38 Loss MOSPD2 GLRA2 FANCB

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