A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602444



Internal ID16389853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32533367..32603062hg38UCSC Ensembl
Innerchr6:32501144..32570839hg19UCSC Ensembl
Innerchr6:32609122..32678817hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3869696
hg1969696
hg1869696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10538n54
Supporting Variantsnssv1055604
Samples
Known GenesHLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602444
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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