A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594457



Internal ID20967528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55177556..55178007hg38UCSC Ensembl
chr14:55644274..55644725hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237811
Samples
Known GenesDLGAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594457
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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