A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096924



Internal ID21291382
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 StatusS
Merged Variantsnsv3114592
Supporting Variants
Samplessample72
Known GenesFAM172A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096924
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