A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602489



Internal ID16389898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32542208..32575067hg38UCSC Ensembl
Innerchr6:32509985..32542844hg19UCSC Ensembl
Innerchr6:32617963..32650822hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3832860
hg1932860
hg1832860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10543n54
Supporting Variantsnssv1055693
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602489
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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