A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495066



Internal ID21152619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58218986..58226766hg38UCSC Ensembl
chr14:58685704..58693484hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg387781
hg197781
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183719
Samples
Known GenesACTR10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495066
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