A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099618



Internal ID21267718
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 StatusS
Merged Variantsnsv3115039
Supporting Variants
Samplessample116
Known GenesLOC284395
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099618
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer