A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589047



Internal ID20962118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58205155..58205452hg38UCSC Ensembl
chr14:58671873..58672170hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237877
Samples
Known GenesACTR10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589047
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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