A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108235



Internal ID21275331
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 StatusS
Merged Variantsnsv3113324
Supporting Variants
Samplessample220
Known GenesANKRD18DP, LMLN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108235
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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