A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115722



Internal ID21298988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:5694320..5697761hg38UCSC Ensembl
Innerchr2:5834452..5837893hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg383442
hg193442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104605
Samplessample136
Known GenesSOX11
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115722
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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