A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115631



Internal ID21298897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:68119858..68123668hg38UCSC Ensembl
Innerchr2:68346990..68350800hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383811
hg193811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106747
Samplessample363
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115631
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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