A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225615



Internal ID20792655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103372459..103372747hg38UCSC Ensembl
chr10:105132216..105132504hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585036
Supporting Variants
Samples
Known GenesTAF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225615
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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