A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590191



Internal ID20963262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69119661..69120303hg38UCSC Ensembl
chr14:69586378..69587020hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237937
Samples
Known GenesDCAF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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