A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055661



Internal ID15908847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32536048..32581804hg38UCSC Ensembl
Innerchr6:32503825..32549581hg19UCSC Ensembl
Innerchr6:32611803..32657559hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3845757
hg1945757
hg1845757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602466
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)nssv1055661
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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