A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602314



Internal ID16389723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32492526..32522114hg38UCSC Ensembl
Innerchr6:32460303..32489891hg19UCSC Ensembl
Innerchr6:32568281..32597869hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3829589
hg1929589
hg1829589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10500n54
Supporting Variantsnssv1054989
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602314
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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