A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117742



Internal ID21301008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27994299..28065966hg38UCSC Ensembl
Innerchr19:28485206..28556873hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg3871668
hg1971668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101940
Samplessample114
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117742
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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