A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476561



Internal ID21134114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58343727..58349611hg38UCSC Ensembl
chr14:58810445..58816329hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg385885
hg195885
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187736
Samples
Known GenesARID4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476561
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