A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245644



Internal ID20812684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45275140..45276188hg38UCSC Ensembl
chr19:45778398..45779446hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598902
Supporting Variants
Samples
Known GenesMARK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245644
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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