A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112630



Internal ID21295896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3454559..3459689hg38UCSC Ensembl
Innerchr16:3504559..3509689hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385131
hg195131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096442
Samplessample289
Known GenesNAA60
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112630
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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