A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1116184



Internal ID15969370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74452293..74454488hg38UCSC Ensembl
Innerchr8:75364528..75366723hg19UCSC Ensembl
Innerchr8:75527083..75529278hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg382196
hg192196
hg182196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611546
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)nssv1116184
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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