A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597386



Internal ID20970457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40085600..40087003hg38UCSC Ensembl
chr19:40591507..40592910hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381404
hg191404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248409
Samples
Known GenesZNF780A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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