A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589198



Internal ID20962269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65557396..65558341hg38UCSC Ensembl
chr14:66024114..66025059hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237430
Samples
Known GenesFUT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589198
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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