A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672372



Internal ID15062338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65389463..65396929hg38UCSC Ensembl
Innerchr15:65681801..65689267hg19UCSC Ensembl
Innerchr15:63468854..63476320hg18UCSC Ensembl
Innerchr15:63468854..63476320hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg387467
hg197467
hg187467
hg177467
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515939
Supporting Variants
Samples
Known GenesIGDCC4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672372
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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