A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682624



Internal ID15072590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34579095hg38UCSC Ensembl
Innerchr15:34718594..34871296hg19UCSC Ensembl
Innerchr15:32505886..32658588hg18UCSC Ensembl
Innerchr15:32505886..32658588hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38152703
hg19152703
hg18152703
hg17152703
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517751
Supporting Variants
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682624
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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