A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602542



Internal ID16389951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32555036..32577369hg38UCSC Ensembl
Innerchr6:32522813..32545146hg19UCSC Ensembl
Innerchr6:32630791..32653124hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3822334
hg1922334
hg1822334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10550n54
Supporting Variantsnssv1055833, nssv1055831, nssv1055830, nssv1055832, nssv1055834
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602542
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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