A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240557



Internal ID20807597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90112417..90189760hg38UCSC Ensembl
chr15:90655649..90732992hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3877344
hg1977344
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582563
Supporting Variants
Samples
Known GenesSEMA4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240557
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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