A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255803



Internal ID20822844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:163663385..163663723hg38UCSC Ensembl
chr2:164519895..164520233hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549853
Supporting Variants
Samples
Known GenesFIGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255803
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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