A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115578



Internal ID21298844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:127700936..127703095hg38UCSC Ensembl
Innerchr2:128458510..128460669hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg382160
hg192160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv645n145
Supporting Variantsnssv14105181, nssv14104868
Samplessample182, sample265
Known GenesSFT2D3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115578
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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