A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032735



Internal ID89517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43165005..43165728hg38UCSC Ensembl
chr10:43660453..43661176hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491892
Supporting Variants
Samples
Known GenesCSGALNACT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032735
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