A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233791



Internal ID20800831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20655338..20655581hg38UCSC Ensembl
chr13:21229477..21229720hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580056
Supporting Variants
Samples
Known GenesIFT88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233791
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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