A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619520



Internal ID21811567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4596343..4607543hg38UCSC Ensembl
chr19:4596355..4607555hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811201
hg1911201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619520
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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