A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1137193



Internal ID15990379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71141615..71152948hg38UCSC Ensembl
Innerchr9:73756531..73767864hg19UCSC Ensembl
Innerchr9:72946351..72957684hg18UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3811334
hg1911334
hg1811334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614602
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1137193
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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