A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245882



Internal ID20812922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31900629..31901998hg38UCSC Ensembl
chr19:32391535..32392904hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381370
hg191370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245882
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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