A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055566



Internal ID15908752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32526201..32658151hg38UCSC Ensembl
Innerchr6:32493978..32625928hg19UCSC Ensembl
Innerchr6:32601956..32733906hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38131951
hg19131951
hg18131951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602425
Supporting Variants
Samples
Known GenesHLA-DQA1, HLA-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)nssv1055566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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