A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108562



Internal ID21284198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113944467..113950823hg38UCSC Ensembl
Innerchr3:113663314..113669670hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg386357
hg196357
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112799
Supporting Variants
Samplessample359
Known GenesGRAMD1C, ZDHHC23
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108562
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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