A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602193



Internal ID16389602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32489473..32584248hg38UCSC Ensembl
Innerchr6:32457250..32552025hg19UCSC Ensembl
Innerchr6:32565228..32660003hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3894776
hg1994776
hg1894776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054534, nssv1054535, nssv1054536
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)nsv602193
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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