A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055906



Internal ID15909092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32562421..32597007hg38UCSC Ensembl
Innerchr6:32530198..32564784hg19UCSC Ensembl
Innerchr6:32638176..32672762hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3834587
hg1934587
hg1834587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602572
Supporting Variants
Samples
Known GenesHLA-DRB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055906
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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