A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602127



Internal ID16389536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32464077..32581498hg38UCSC Ensembl
Innerchr6:32431854..32549275hg19UCSC Ensembl
Innerchr6:32539832..32657253hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38117422
hg19117422
hg18117422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10488n54
Supporting Variantsnssv1053930, nssv1053931
Samples
Known GenesHLA-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)nsv602127
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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