A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055604



Internal ID15908790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32533367..32603062hg38UCSC Ensembl
Innerchr6:32501144..32570839hg19UCSC Ensembl
Innerchr6:32609122..32678817hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3869696
hg1969696
hg1869696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602444
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)nssv1055604
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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