A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1116159



Internal ID15969345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:72327795..72409991hg38UCSC Ensembl
Innerchr8:73240030..73322226hg19UCSC Ensembl
Innerchr8:73402584..73484780hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3882197
hg1982197
hg1882197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611532
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)nssv1116159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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