A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593393



Internal ID20966464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67258315..67258604hg38UCSC Ensembl
chr14:67725032..67725321hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237463
Samples
Known GenesMPP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593393
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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