A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601687



Internal ID16389096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31315520..31383665hg38UCSC Ensembl
Innerchr6:31283297..31351442hg19UCSC Ensembl
Innerchr6:31391276..31459421hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3868146
hg1968146
hg1868146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053056
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)nsv601687
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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