A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111205



Internal ID21294471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79972074..79975400hg38UCSC Ensembl
Innerchr16:80005971..80009297hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg383327
hg193327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096426
Samplessample276
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111205
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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