A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599887



Internal ID20972958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52229268..52230330hg38UCSC Ensembl
chr19:52732521..52733583hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg381063
hg191063
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599887
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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