A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660243



Internal ID15050209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34464224hg38UCSC Ensembl
Innerchr15:34718594..34756425hg19UCSC Ensembl
Innerchr15:32505886..32543717hg18UCSC Ensembl
Innerchr15:32505886..32543717hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3837832
hg1937832
hg1837832
hg1737832
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517751
Supporting Variants
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660243
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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