A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1137191



Internal ID15990377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71140686..71150994hg38UCSC Ensembl
Innerchr9:73755602..73765910hg19UCSC Ensembl
Innerchr9:72945422..72955730hg18UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3810309
hg1910309
hg1810309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614600
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)nssv1137191
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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