A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657934



Internal ID15394586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56193400..56204384hg38UCSC Ensembl
Innerchr15:56485598..56496582hg19UCSC Ensembl
Innerchr15:54272890..54283874hg18UCSC Ensembl
Innerchr15:54272890..54283874hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3810985
hg1910985
hg1810985
hg1710985
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519725
Supporting Variants
Samples
Known GenesRFX7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657934
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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