A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031793



Internal ID88914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25473000..25482000hg38UCSC Ensembl
chr10:25761929..25770929hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg389001
hg199001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488085
Supporting Variants
Samples
Known GenesGPR158
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031793
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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