A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598255



Internal ID20971326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57521385..57521704hg38UCSC Ensembl
chr19:58032753..58033072hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598255
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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