A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176488



Internal ID15876421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:119840800..119878141hg38UCSC Ensembl
Innerchr9:122603078..122640419hg19UCSC Ensembl
Innerchr9:121642899..121680240hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3837342
hg1937342
hg1837342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615269
Supporting Variants
SamplesHGDP00837
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176488
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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