A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103741



Internal ID21293271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:127700936..127702939hg38UCSC Ensembl
Innerchr2:128458510..128460513hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg382004
hg192004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111586
Supporting Variants
Samplessample98
Known GenesSFT2D3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103741
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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