A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106747



Internal ID21284673
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 StatusS
Merged Variantsnsv3115631
Supporting Variants
Samplessample363
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106747
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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