A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089772



Internal ID21282512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102196367..102211837hg38UCSC Ensembl
Innerchr10:103956124..103971594hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3815471
hg1915471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115524
Supporting Variants
Samplessample328
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089772
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