A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189649



Internal ID20756689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:65966982..65978725hg38UCSC Ensembl
chr13:66541114..66552857hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3811744
hg1911744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189649
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