A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476846



Internal ID21134399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23580826..23601770hg38UCSC Ensembl
chr14:24050035..24070979hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3820945
hg1920945
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476846
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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