A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112897



Internal ID21296163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51749429..51753661hg38UCSC Ensembl
Innerchr15:52041626..52045858hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg384233
hg194233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv405n145
Supporting Variantsnssv14097084
Samplessample289
Known GenesLYSMD2, TMOD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112897
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