A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720561



Internal ID144227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3301157..3341296hg38UCSC Ensembl
chr19:3301155..3341294hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3840140
hg1940140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533236
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720561
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer