A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096233



Internal ID21272751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93597300..93626404hg38UCSC Ensembl
Innerchr15:94140529..94169633hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3829105
hg1929105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111845
Supporting Variants
Samplessample181
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096233
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