A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117980



Internal ID21301246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34209118..34210757hg38UCSC Ensembl
Innerchr15:34501319..34502958hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381640
hg191640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097169
Samplessample348
Known GenesKATNBL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117980
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