A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695841



Internal ID15432493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23403645..23448259hg38UCSC Ensembl
Innerchr15:23648792..23693406hg19UCSC Ensembl
Innerchr15:21200233..21244499hg18UCSC Ensembl
Innerchr15:21200233..21244499hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3844615
hg1944615
hg1844267
hg1744267
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518410
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695841
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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