A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090145



Internal ID21268914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:118416188..118419655hg38UCSC Ensembl
Innerchr10:120175700..120179167hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383468
hg193468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111820
Supporting Variants
Samplessample131
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090145
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