A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115039



Internal ID21298305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29498854..29502939hg38UCSC Ensembl
Innerchr19:29989761..29993846hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg384086
hg194086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099618
Samplessample116
Known GenesLOC284395
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115039
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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