A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701936



Internal ID15438588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55173957..55193296hg38UCSC Ensembl
Innerchr15:55466155..55485494hg19UCSC Ensembl
Innerchr15:53253447..53272786hg18UCSC Ensembl
Innerchr15:53253447..53272786hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3819340
hg1919340
hg1819340
hg1719340
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525768
Supporting Variants
Samples
Known GenesRSL24D1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701936
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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