A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595784



Internal ID20968855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16432659..16433093hg38UCSC Ensembl
chr19:16543470..16543904hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247550
Samples
Known GenesEPS15L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595784
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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