A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117621



Internal ID21300887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:59802825..59808197hg38UCSC Ensembl
Innerchr16:59836729..59842101hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385373
hg195373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098268, nssv14096550
Samplessample38, sample358
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117621
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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