A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113324



Internal ID21296590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:198030509..198150051hg38UCSC Ensembl
Innerchr3:197757380..197876922hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38119543
hg19119543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107990, nssv14108235
Samplessample220, sample316
Known GenesANKRD18DP, LMLN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113324
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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