A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057622



Internal ID15564122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32998165..33150041hg38UCSC Ensembl
Innerchr6:32965942..33117818hg19UCSC Ensembl
Innerchr6:33073920..33225796hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38151877
hg19151877
hg18151877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602818
Supporting Variants
Samples
Known GenesHLA-DOA, HLA-DPA1, HLA-DPB1, HLA-DPB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057622
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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