A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1054860



Internal ID15908046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32583827hg38UCSC Ensembl
Innerchr6:32458912..32551604hg19UCSC Ensembl
Innerchr6:32566890..32659582hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3892693
hg1992693
hg1892693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602266
Supporting Variants
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)nssv1054860
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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