A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703395



Internal ID15440047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53683970..53684200hg38UCSC Ensembl
Innerchr15:53976167..53976397hg19UCSC Ensembl
Innerchr15:51763459..51763689hg18UCSC Ensembl
Innerchr15:51763459..51763689hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38231
hg19231
hg18231
hg17231
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527020
Supporting Variants
Samples
Known GenesWDR72
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703395
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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