A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602140



Internal ID16389549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32475674..32601910hg38UCSC Ensembl
Innerchr6:32443451..32569687hg19UCSC Ensembl
Innerchr6:32551429..32677665hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38126237
hg19126237
hg18126237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10492n54
Supporting Variantsnssv1053948, nssv1053950, nssv1053949
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)nsv602140
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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