A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241130



Internal ID20808170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57300482..57301134hg38UCSC Ensembl
chr15:57592680..57593332hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591077
Supporting Variants
Samples
Known GenesLINC00926
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241130
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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