A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602463



Internal ID16389872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32534102..32687441hg38UCSC Ensembl
Innerchr6:32501879..32655218hg19UCSC Ensembl
Innerchr6:32609857..32763196hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38153340
hg19153340
hg18153340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055658
Samples
Known GenesHLA-DQA1, HLA-DQB1, HLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602463
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer