A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697988



Internal ID121654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76953005..76955292hg38UCSC Ensembl
chr14:77419348..77421635hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382288
hg192288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697988
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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