A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594809



Internal ID20967880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63658242..63659387hg38UCSC Ensembl
chr14:64124960..64126105hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594809
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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