A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106391



Internal ID21269662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183252088..183256267hg38UCSC Ensembl
Innerchr3:182969876..182974055hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg384180
hg194180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117304
Supporting Variants
Samplessample141
Known GenesB3GNT5, MCF2L2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106391
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