A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602539



Internal ID16389948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32555036..32564146hg38UCSC Ensembl
Innerchr6:32522813..32531923hg19UCSC Ensembl
Innerchr6:32630791..32639901hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg389111
hg199111
hg189111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10557n54
Supporting Variantsnssv1055824
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602539
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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