A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187190



Internal ID20754230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36628920..36630910hg38UCSC Ensembl
chr13:37203057..37205047hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381991
hg191991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482048
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187190
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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