A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213634



Internal ID20780674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41305452..41308878hg38UCSC Ensembl
chr4:41307469..41310895hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg383427
hg193427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213634
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