A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038536



Internal ID93425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76060881..76060943hg38UCSC Ensembl
chr10:77820639..77820701hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491447
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038536
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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