A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102402



Internal ID21287928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:59394018..59397260hg38UCSC Ensembl
Innerchr2:59621153..59624395hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115649
Supporting Variants
Samplessample41
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102402
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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