A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602522



Internal ID16389931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32554310..32579086hg38UCSC Ensembl
Innerchr6:32522087..32546863hg19UCSC Ensembl
Innerchr6:32630065..32654841hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3824777
hg1924777
hg1824777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10550n54
Supporting Variantsnssv1055760
Samples
Known GenesHLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602522
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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