A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186954



Internal ID20753994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58851990..58872414hg38UCSC Ensembl
chr15:59144189..59164613hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg3820425
hg1920425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509265
Supporting Variants
Samples
Known GenesFAM63B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186954
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