A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106071



Internal ID21280399
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 StatusS
Merged Variantsnsv3113959
Supporting Variants
Samplessample297
Known GenesSH3RF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106071
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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