A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197185



Internal ID20764225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73754395..74187990hg38UCSC Ensembl
chr18:71421630..71855225hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38433596
hg19433596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516656
Supporting Variants
Samples
Known GenesFBXO15, TIMM21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197185
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