A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268763



Internal ID20835803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154874384..154874721hg38UCSC Ensembl
chr5:154253944..154254281hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571790
Supporting Variants
Samples
Known GenesCNOT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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