A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101384



Internal ID21281564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35167717..35174589hg38UCSC Ensembl
Innerchr19:35658620..35665492hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386873
hg196873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111832
Supporting Variants
Samplessample313
Known GenesFXYD5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101384
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