A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225256



Internal ID20792296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45246951..45248020hg38UCSC Ensembl
chr13:45821086..45822155hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg381070
hg191070
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578253
Supporting Variants
Samples
Known GenesGTF2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225256
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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