A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602597



Internal ID16390006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32572508..32685658hg38UCSC Ensembl
Innerchr6:32540285..32653435hg19UCSC Ensembl
Innerchr6:32648263..32761413hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38113151
hg19113151
hg18113151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10567n54
Supporting Variantsnssv1055974
Samples
Known GenesHLA-DQA1, HLA-DQB1, HLA-DRB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602597
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