A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241986



Internal ID20809026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75584850..75585979hg38UCSC Ensembl
chr15:75877191..75878320hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg381130
hg191130
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587196
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241986
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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