A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106451



Internal ID21270327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179449461..179452803hg38UCSC Ensembl
Innerchr3:179167249..179170591hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg383343
hg193343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116992
Supporting Variants
Samplessample149
Known GenesGNB4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106451
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