A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239068



Internal ID20806108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93115534..93486112hg38UCSC Ensembl
chr15:93658763..94029341hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38370579
hg19370579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239068
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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