A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247546



Internal ID20814586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16263253..16264064hg38UCSC Ensembl
chr19:16374064..16374875hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38812
hg19812
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597273
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247546
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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