A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241888



Internal ID20808928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72521648..72522349hg38UCSC Ensembl
chr15:72813989..72814690hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594664
Supporting Variants
Samples
Known GenesARIH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241888
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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