A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031768



Internal ID88900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25233789..25234058hg38UCSC Ensembl
chr10:25522718..25522987hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479801
Supporting Variants
Samples
Known GenesGPR158
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031768
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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