A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218800



Internal ID20785840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109066801..109075000hg38UCSC Ensembl
chr8:110079030..110087229hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218800
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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