A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602137



Internal ID16389546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32474926..32531237hg38UCSC Ensembl
Innerchr6:32442703..32499014hg19UCSC Ensembl
Innerchr6:32550681..32606992hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3856312
hg1956312
hg1856312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10493n54
Supporting Variantsnssv1053941
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602137
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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