A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038344



Internal ID93291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86692224..86692353hg38UCSC Ensembl
chr10:88451981..88452110hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483264
Supporting Variants
Samples
Known GenesLDB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038344
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008742


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