A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053074



Internal ID15906260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31316567..31370583hg38UCSC Ensembl
Innerchr6:31284344..31338360hg19UCSC Ensembl
Innerchr6:31392323..31446339hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3854017
hg1954017
hg1854017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601704
Supporting Variants
Samples
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053074
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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