A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594201



Internal ID20967272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58574072..58574888hg38UCSC Ensembl
chr14:59040790..59041606hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594201
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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