A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591401



Internal ID20964472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68868616..68868968hg38UCSC Ensembl
chr14:69335333..69335685hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591401
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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