A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267412



Internal ID20834452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159190112..159190616hg38UCSC Ensembl
chr5:158617120..158617624hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570424
Supporting Variants
Samples
Known GenesRNF145
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267412
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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