A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693631



Internal ID15430283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84645608..84657523hg38UCSC Ensembl
Innerchr15:85188839..85200754hg19UCSC Ensembl
Innerchr15:82989843..83001758hg18UCSC Ensembl
Innerchr15:82989843..83001758hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3811916
hg1911916
hg1811916
hg1711916
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515983
Supporting Variants
Samples
Known GenesNMB, WDR73
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693631
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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