A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031770



Internal ID88902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25241295..25256945hg38UCSC Ensembl
chr10:25530224..25545874hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3815651
hg1915651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480550
Supporting Variants
Samples
Known GenesGPR158
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031770
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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