A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602376



Internal ID16389785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32506157..32652845hg38UCSC Ensembl
Innerchr6:32473934..32620622hg19UCSC Ensembl
Innerchr6:32581912..32728600hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38146689
hg19146689
hg18146689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10489n54
Supporting Variantsnssv1055285
Samples
Known GenesHLA-DQA1, HLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602376
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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