A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247554



Internal ID20814594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16479954..16481594hg38UCSC Ensembl
chr19:16590765..16592405hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381641
hg191641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598693
Supporting Variants
Samples
Known GenesCALR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247554
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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