A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114592



Internal ID21297858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93791319..93797292hg38UCSC Ensembl
Innerchr5:93127025..93132998hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg385974
hg195974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096924
Samplessample72
Known GenesFAM172A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114592
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