A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241169



Internal ID20808209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58894883..58896381hg38UCSC Ensembl
chr15:59187082..59188580hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591452
Supporting Variants
Samples
Known GenesSLTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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