A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421199



Internal ID22479069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35784357..35837624hg38UCSC Ensembl
chr4:35785979..35839246hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3853268
hg1953268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901406
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421199
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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