A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249091



Internal ID20816131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5748369..5748949hg38UCSC Ensembl
chr19:5748380..5748960hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596701
Supporting Variants
Samples
Known GenesCATSPERD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249091
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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