A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250238



Internal ID20817278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192830119..193074178hg38UCSC Ensembl
chr1:192799249..193043308hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38244060
hg19244060
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540558
Supporting Variants
Samples
Known GenesTROVE2, UCHL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250238
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.03966


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