A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246692



Internal ID20813732
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 StatusS
Merged Variantsnsv6599887
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246692
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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