A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113537



Internal ID21296803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52010122..52038976hg38UCSC Ensembl
Innerchr2:52237260..52266114hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3828855
hg1928855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104677
Samplessample147
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113537
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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