A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117795



Internal ID21301061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62614004..62626071hg38UCSC Ensembl
Innerchr15:62906203..62918270hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3812068
hg1912068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096109
Samplessample122
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117795
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