A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107243



Internal ID21277290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:153242134..153246547hg38UCSC Ensembl
Innerchr4:154163286..154167699hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg384414
hg194414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112145
Supporting Variants
Samplessample25
Known GenesTRIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107243
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