A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055603



Internal ID15908789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32533367..32597554hg38UCSC Ensembl
Innerchr6:32501144..32565331hg19UCSC Ensembl
Innerchr6:32609122..32673309hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3864188
hg1964188
hg1864188
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602443
Supporting Variants
Samples
Known GenesHLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055603
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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