A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588453



Internal ID20961524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75755094..75756675hg38UCSC Ensembl
chr14:76221437..76223018hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381582
hg191582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237471
Samples
Known GenesTTLL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588453
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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