A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209525



Internal ID20776565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110200873..110212536hg38UCSC Ensembl
chr4:111122029..111133692hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3811664
hg1911664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6382306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209525
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