A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033556



Internal ID90062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45690265..45764265hg38UCSC Ensembl
chr10:46185713..46259713hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3874001
hg1974001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491376
Supporting Variants
Samples
Known GenesFAM21C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033556
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001268


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