A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576456



Internal ID20949527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89798788..89800200hg38UCSC Ensembl
chr14:90265132..90266544hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381413
hg191413
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237630
Samples
Known GenesEFCAB11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576456
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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