A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055232



Internal ID15908418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32505386..32521324hg38UCSC Ensembl
Innerchr6:32473163..32489101hg19UCSC Ensembl
Innerchr6:32581141..32597079hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3815939
hg1915939
hg1815939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602359
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)nssv1055232
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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