A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089104



Internal ID21266736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17268103..17273264hg38UCSC Ensembl
Innerchr10:17310102..17315263hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg385162
hg195162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111320
Supporting Variants
Samplessample101
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089104
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