A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188826



Internal ID20755866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33518108..34009759hg38UCSC Ensembl
chr18:31098072..31589723hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38491652
hg19491652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519526
Supporting Variants
Samples
Known GenesASXL3, NOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188826
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