A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055711



Internal ID15908897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32551495..32616832hg38UCSC Ensembl
Innerchr6:32519272..32584609hg19UCSC Ensembl
Innerchr6:32627250..32692587hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3865338
hg1965338
hg1865338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602505
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)nssv1055711
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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