A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602494



Internal ID16389903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32549621..32575763hg38UCSC Ensembl
Innerchr6:32517398..32543540hg19UCSC Ensembl
Innerchr6:32625376..32651518hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3826143
hg1926143
hg1826143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10546n54
Supporting Variantsnssv1055699, nssv1055698
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602494
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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