A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106033



Internal ID21279776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:127700936..127703109hg38UCSC Ensembl
Innerchr2:128458510..128460683hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg382174
hg192174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115438
Supporting Variants
Samplessample289
Known GenesSFT2D3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106033
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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