A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602266



Internal ID16389675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32583827hg38UCSC Ensembl
Innerchr6:32458912..32551604hg19UCSC Ensembl
Innerchr6:32566890..32659582hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3892693
hg1992693
hg1892693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054859, nssv1054860
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)nsv602266
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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