A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602213



Internal ID16389622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32490550..32582545hg38UCSC Ensembl
Innerchr6:32458327..32550322hg19UCSC Ensembl
Innerchr6:32566305..32658300hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3891996
hg1991996
hg1891996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054601
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)nsv602213
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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