A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245657



Internal ID20812697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45749935..45750404hg38UCSC Ensembl
chr19:46253193..46253662hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596098
Supporting Variants
Samples
Known GenesLOC388553
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245657
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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