A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694199



Internal ID117865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110973155..111020017hg38UCSC Ensembl
chr13:111625502..111672364hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3846863
hg1946863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513540
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694199
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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