A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213998



Internal ID20781038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4835801..4841700hg38UCSC Ensembl
chr5:4835914..4841813hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383823
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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