A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209469



Internal ID20776509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104643643..104657276hg38UCSC Ensembl
chr4:105564800..105578433hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3813634
hg1913634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209469
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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