A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118275



Internal ID21301541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32444783..32626512hg38UCSC Ensembl
Innerchr6:32412560..32594289hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38181730
hg19181730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1023n145
Supporting Variantsnssv14083534, nssv14089188, nssv14083808, nssv14083701, nssv14083008, nssv14083606, nssv14087699, nssv14087751, nssv14082814
Samplessample382, sample29, sample216, sample231, sample61, sample6, sample43, sample278, sample335
Known GenesHLA-DRA, HLA-DRB1, HLA-DRB5, HLA-DRB6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118275
Frequency
Sample Size467
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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