A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602291



Internal ID16389700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491421..32519533hg38UCSC Ensembl
Innerchr6:32459198..32487310hg19UCSC Ensembl
Innerchr6:32567176..32595288hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3828113
hg1928113
hg1828113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10500n54
Supporting Variantsnssv1054957
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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