A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602128



Internal ID16389537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32465982..32551495hg38UCSC Ensembl
Innerchr6:32433759..32519272hg19UCSC Ensembl
Innerchr6:32541737..32627250hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3885514
hg1985514
hg1885514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10491n54
Supporting Variantsnssv1053932
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602128
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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