A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663211



Internal ID15053177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34506266hg38UCSC Ensembl
Innerchr15:34718594..34798467hg19UCSC Ensembl
Innerchr15:32505886..32585759hg18UCSC Ensembl
Innerchr15:32505886..32585759hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3879874
hg1979874
hg1879874
hg1779874
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)nssv663211
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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