A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703637



Internal ID15440289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75012699..75028921hg38UCSC Ensembl
Innerchr15:75305040..75321262hg19UCSC Ensembl
Innerchr15:73092093..73108315hg18UCSC Ensembl
Innerchr15:73092093..73108315hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3816223
hg1916223
hg1816223
hg1716223
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527237
Supporting Variants
Samples
Known GenesPPCDC, SCAMP5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703637
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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