A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602257



Internal ID16389666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32555036hg38UCSC Ensembl
Innerchr6:32458912..32522813hg19UCSC Ensembl
Innerchr6:32566890..32630791hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3863902
hg1963902
hg1863902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10503n54
Supporting Variantsnssv1054806
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602257
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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