A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111586



Internal ID21294852
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 StatusM
Merged Variantsdgv645n145
Supporting Variantsnssv14103741, nssv14105879
Samplessample98, sample246
Known GenesSFT2D3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111586
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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