A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602229



Internal ID16389638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491063..32522114hg38UCSC Ensembl
Innerchr6:32458840..32489891hg19UCSC Ensembl
Innerchr6:32566818..32597869hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3831052
hg1931052
hg1831052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10499n54
Supporting Variantsnssv1054643, nssv1054644
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602229
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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