A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115524



Internal ID21298790
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 StatusM
Merged Variantsdgv176n145
Supporting Variantsnssv14089772
Samplessample328
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115524
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