A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598205



Internal ID20971276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49563604..49564218hg38UCSC Ensembl
chr19:50066861..50067475hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246628
Samples
Known GenesNOSIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598205
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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