A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602152



Internal ID16389561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32484256..32564146hg38UCSC Ensembl
Innerchr6:32452033..32531923hg19UCSC Ensembl
Innerchr6:32560011..32639901hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3879891
hg1979891
hg1879891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10491n54
Supporting Variantsnssv1053962
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)nsv602152
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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