A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602135



Internal ID16389544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32473615..32677082hg38UCSC Ensembl
Innerchr6:32441392..32644859hg19UCSC Ensembl
Innerchr6:32549370..32752837hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38203468
hg19203468
hg18203468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10494n54
Supporting Variantsnssv1053939
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)nsv602135
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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