A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602232



Internal ID16389641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491063..32592381hg38UCSC Ensembl
Innerchr6:32458840..32560158hg19UCSC Ensembl
Innerchr6:32566818..32668136hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38101319
hg19101319
hg18101319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10505n54
Supporting Variantsnssv1054651, nssv1054650
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)nsv602232
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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