A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1054902



Internal ID15908088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32592608hg38UCSC Ensembl
Innerchr6:32458912..32560385hg19UCSC Ensembl
Innerchr6:32566890..32668363hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38101474
hg19101474
hg18101474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602270
Supporting Variants
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1054902
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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