A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267411



Internal ID20834451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159161152..159168041hg38UCSC Ensembl
chr5:158588160..158595049hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg386890
hg196890
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571344
Supporting Variants
Samples
Known GenesRNF145
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267411
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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