A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088730



Internal ID21279740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45000185..45001983hg38UCSC Ensembl
Innerchr10:45495633..45497431hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381799
hg191799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118104
Supporting Variants
Samplessample289
Known GenesC10orf25, ZNF22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088730
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