A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215739



Internal ID20782779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26437614..26439280hg38UCSC Ensembl
chr5:26437723..26439389hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg381667
hg191667
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395239
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215739
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