A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488768



Internal ID266065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25185156..25201896hg38UCSC Ensembl
chr10:25474085..25490825hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3816741
hg1916741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031760
Samples
Known GenesGPR158
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488768
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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