A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591288



Internal ID20964359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74332524..74333373hg38UCSC Ensembl
chr14:74799227..74800076hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591288
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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