A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116130



Internal ID21299396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24927528..24937879hg38UCSC Ensembl
Innerchr2:25150397..25160748hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3810352
hg1910352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104823
Samplessample173
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116130
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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