A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156905



Internal ID15872697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23171517..23185204hg38UCSC Ensembl
Innerchr9:23171516..23185202hg19UCSC Ensembl
Innerchr9:23161516..23175202hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3813688
hg1913687
hg1813687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613791
Supporting Variants
SamplesHGDP00019
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156905
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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