A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239483



Internal ID20806523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30937510..30938077hg38UCSC Ensembl
chr15:31229713..31230280hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590286
Supporting Variants
Samples
Known GenesFAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239483
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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