A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602350



Internal ID16389759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32504326..32562421hg38UCSC Ensembl
Innerchr6:32472103..32530198hg19UCSC Ensembl
Innerchr6:32580081..32638176hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3858096
hg1958096
hg1858096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10522n54
Supporting Variantsnssv1055219
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602350
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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