A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113874



Internal ID21297140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:183036609..183039945hg38UCSC Ensembl
Innerchr2:183901337..183904673hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg383337
hg193337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv658n145
Supporting Variantsnssv14106314
Samplessample349
Known GenesNCKAP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113874
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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