A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17007377



Internal ID72557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10337385..10339789hg38UCSC Ensembl
chr8:10194895..10197299hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382405
hg192405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488585
Supporting Variants
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17007377
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer