A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602230



Internal ID16389639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491063..32578591hg38UCSC Ensembl
Innerchr6:32458840..32546368hg19UCSC Ensembl
Innerchr6:32566818..32654346hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3887529
hg1987529
hg1887529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10505n54
Supporting Variantsnssv1054645
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)nsv602230
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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