A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101266



Internal ID21278765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29940208..29950749hg38UCSC Ensembl
Innerchr19:30431115..30441656hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3810542
hg1910542
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113170
Supporting Variants
Samplessample273
Known GenesURI1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101266
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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