A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602384



Internal ID16389793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32510377..32540452hg38UCSC Ensembl
Innerchr6:32478154..32508229hg19UCSC Ensembl
Innerchr6:32586132..32616207hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3830076
hg1930076
hg1830076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10521n54
Supporting Variantsnssv1055360, nssv1055359
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602384
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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