A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214493



Internal ID20781533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135865030..135892771hg38UCSC Ensembl
chr5:135200719..135228460hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3827742
hg1927742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407233
Supporting Variants
Samples
Known GenesIL9, SLC25A48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214493
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