A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115713



Internal ID21298979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:99303024..99307514hg38UCSC Ensembl
Innerchr10:101062781..101067271hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg384491
hg194491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv174n145
Supporting Variantsnssv14088560
Samplessample198
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115713
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