A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210445



Internal ID20777485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24689834..24716671hg38UCSC Ensembl
chr3:24731325..24758162hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3826838
hg1926838
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367711
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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