A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031759



Internal ID88894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25164478..25164631hg38UCSC Ensembl
chr10:25453407..25453560hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493910
Supporting Variants
Samples
Known GenesGPR158-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031759
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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