A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246260



Internal ID20813300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21285497..21286409hg38UCSC Ensembl
chr19:21468299..21469211hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598352
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246260
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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