A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249102



Internal ID20816142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57662682..57663462hg38UCSC Ensembl
chr19:58174050..58174830hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597866
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249102
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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