A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106847



Internal ID21286097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13372589..13420577hg38UCSC Ensembl
Innerchr2:13512714..13560702hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3847989
hg1947989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118033
Supporting Variants
Samplessample383
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106847
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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