A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1054976



Internal ID15908162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491715..32540452hg38UCSC Ensembl
Innerchr6:32459492..32508229hg19UCSC Ensembl
Innerchr6:32567470..32616207hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3848738
hg1948738
hg1848738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602302
Supporting Variants
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1054976
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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