A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148990



Internal ID15529226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34506266hg38UCSC Ensembl
Innerchr15:34718594..34798467hg19UCSC Ensembl
Innerchr15:32505886..32585759hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3879874
hg1979874
hg1879874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568996
Supporting Variants
SamplesHGDP00756
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148990
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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