A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602133



Internal ID16389542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32473615..32553010hg38UCSC Ensembl
Innerchr6:32441392..32520787hg19UCSC Ensembl
Innerchr6:32549370..32628765hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3879396
hg1979396
hg1879396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10491n54
Supporting Variantsnssv1053937
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602133
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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