A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156745



Internal ID15879225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26643037..26689444hg38UCSC Ensembl
Innerchr9:26643035..26689442hg19UCSC Ensembl
Innerchr9:26633035..26679442hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3846408
hg1946408
hg1846408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613940
Supporting Variants
SamplesHGDP01330
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156745
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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