A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111956



Internal ID21295222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:25873167..25876512hg38UCSC Ensembl
Innerchr10:26162096..26165441hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383346
hg193346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv153n145
Supporting Variantsnssv14088594
Samplessample216
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111956
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