A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239388



Internal ID20806428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24980406..24981563hg38UCSC Ensembl
chr15:25225553..25226710hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381158
hg191158
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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