A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113959



Internal ID21297225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:109315739..109317796hg38UCSC Ensembl
Innerchr2:109932195..109934252hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg382058
hg192058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106071
Samplessample297
Known GenesSH3RF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113959
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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