A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101103



Internal ID21287325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31864455..31913370hg38UCSC Ensembl
Innerchr19:32355361..32404276hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3848916
hg1948916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111451
Supporting Variants
Samplessample40
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101103
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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