A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086359



Internal ID21268670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32444783..32561883hg38UCSC Ensembl
Innerchr6:32412560..32529660hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38117101
hg19117101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113731
Supporting Variants
Samplessample129
Known GenesHLA-DRA, HLA-DRB5, HLA-DRB6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086359
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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