A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102909



Internal ID21287574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46434454..46441919hg38UCSC Ensembl
Innerchr19:46937711..46945176hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg387466
hg197466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117344
Supporting Variants
Samplessample403
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102909
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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