A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106332



Internal ID21283987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:80934420..81020210hg38UCSC Ensembl
Innerchr2:81161544..81247334hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3885791
hg1985791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117991
Supporting Variants
Samplessample354
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106332
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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