A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526136



Internal ID15453429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37696562..37820873hg38UCSC Ensembl
Innerchr7:37736164..37860475hg19UCSC Ensembl
Innerchr7:37702689..37827000hg18UCSC Ensembl
Innerchr7:37509404..37633715hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38124312
hg19124312
hg18124312
hg17124312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702391
Samples
Known GenesGPR141
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526136
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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