A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238282



Internal ID20805322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40896809..40898266hg38UCSC Ensembl
chr15:41189007..41190464hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582487
Supporting Variants
Samples
Known GenesVPS18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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