A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602147



Internal ID16389556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32477873..32539789hg38UCSC Ensembl
Innerchr6:32445650..32507566hg19UCSC Ensembl
Innerchr6:32553628..32615544hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3861917
hg1961917
hg1861917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10493n54
Supporting Variantsnssv1053957
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602147
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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