A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602345



Internal ID16389754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32501683..32621031hg38UCSC Ensembl
Innerchr6:32469460..32588808hg19UCSC Ensembl
Innerchr6:32577438..32696786hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38119349
hg19119349
hg18119349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10492n54
Supporting Variantsnssv1055179
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602345
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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