A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182814



Internal ID20749854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63387501..63398700hg38UCSC Ensembl
chr13:63961634..63972833hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3811200
hg1911200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182814
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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