A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266197



Internal ID20833237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121385551..121883506hg38UCSC Ensembl
chr5:120721246..121219201hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38497956
hg19497956
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564826
Supporting Variants
Samples
Known GenesFTMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266197
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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