A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268985



Internal ID20836025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80520657..80521055hg38UCSC Ensembl
chr5:79816476..79816874hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556478
Supporting Variants
Samples
Known GenesFAM151B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268985
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00032


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