Product Details

Assay Reference Genome
Location

Chr.4:186210415 on build GRCh38
Cytoband
4q35.2
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs72646297] 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
285440
Gene Symbol
CYP4V2
Gene Name
cytochrome P450 family 4 subfamily V member 2
Gene Aliases
BCD, CYP4AH1
Location
Chr.4:186191520-186213463 on build GRCh38
Assay Gene Location
Overlaps Intron 10 - Exon 11
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
CYP4V2 NM_207352.3 NP_997235.3
XM_005262935.3 XP_005262992.1
XM_017008037.1 XP_016863526.1
AK022114.1
AK122600.1 BAC85487.1
AK126473.1 BAC86562.1
AK311390.1
AY422002.1 AAR31180.1
BC041839.1 AAH41839.1
BC060857.1 AAH60857.1
BX648537.1
BX648730.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv3894090 Chr4:186011626 - 186212421 on Build GRCh38 Gain TLR3 FLJ38576 FAM149A CYP4V2
nsv1028146 Chr4:185582745 - 186417181 on Build GRCh38 Gain F11-AS1 F11 SORBS2 TLR3 KLKB1 FLJ38576 FAM149A CYP4V2
nsv4644 Chr4:186185600 - 186219291 on Build GRCh38 Insertion KLKB1 FLJ38576 CYP4V2
nsv830172 Chr4:186091611 - 186247270 on Build GRCh38 Loss KLKB1 FLJ38576 FAM149A CYP4V2
nsv508340 Chr4:186138019 - 186215804 on Build GRCh38 Deletion KLKB1 FLJ38576 FAM149A CYP4V2
esv3603523 Chr4:186176579 - 186214960 on Build GRCh38 Gain FLJ38576 CYP4V2
nsv461864 Chr4:186085652 - 186335850 on Build GRCh38 Gain F11-AS1 F11 TLR3 KLKB1 FLJ38576 FAM149A CYP4V2
nsv596401 Chr4:186151229 - 186445495 on Build GRCh38 Loss F11-AS1 F11 KLKB1 FLJ38576 FAM149A CYP4V2
esv3603517 Chr4:186008703 - 186213065 on Build GRCh38 Gain TLR3 FLJ38576 FAM149A CYP4V2
dgv1052e214 Chr4:186072002 - 186212619 on Build GRCh38 Gain TLR3 FLJ38576 FAM149A CYP4V2
nsv4642 Chr4:186164028 - 186215260 on Build GRCh38 Deletion FLJ38576 FAM149A CYP4V2
esv3603525 Chr4:186210472 - 186225457 on Build GRCh38 Loss KLKB1 CYP4V2

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