A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598745



Internal ID20971816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19620156..19621953hg38UCSC Ensembl
chr19:19730965..19732762hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381798
hg191798
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598745
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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