A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1116175



Internal ID15969361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74452293..74454285hg38UCSC Ensembl
Innerchr8:75364528..75366520hg19UCSC Ensembl
Innerchr8:75527083..75529075hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381993
hg191993
hg181993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611545
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)nssv1116175
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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