A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691410



Internal ID115076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77316703..77316765hg38UCSC Ensembl
chr13:77890838..77890900hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503443
Supporting Variants
Samples
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691410
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.011097


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