A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240493



Internal ID20807533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85701628..85702182hg38UCSC Ensembl
chr15:86244859..86245413hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595455
Supporting Variants
Samples
Known GenesAKAP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240493
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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