A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117344



Internal ID21300610
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 StatusM
Merged Variants
Supporting Variantsnssv14102909
Samplessample403
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117344
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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