A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055802



Internal ID15908988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32554937..32555699hg38UCSC Ensembl
Innerchr6:32522714..32523476hg19UCSC Ensembl
Innerchr6:32630692..32631454hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38763
hg19763
hg18763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602533
Supporting Variants
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055802
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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