A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602378



Internal ID16389787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32506157..32687441hg38UCSC Ensembl
Innerchr6:32473934..32655218hg19UCSC Ensembl
Innerchr6:32581912..32763196hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38181285
hg19181285
hg18181285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10489n54
Supporting Variantsnssv1055289
Samples
Known GenesHLA-DQA1, HLA-DQB1, 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)nsv602378
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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