A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602218



Internal ID16389627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32490550..32592485hg38UCSC Ensembl
Innerchr6:32458327..32560262hg19UCSC Ensembl
Innerchr6:32566305..32668240hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38101936
hg19101936
hg18101936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10506n54
Supporting Variantsnssv1054607, nssv1054610, nssv1054608, nssv1054609
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)nsv602218
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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