A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252627



Internal ID20819667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5111452..5112132hg38UCSC Ensembl
chr20:5092098..5092778hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38681
hg19681
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597984
Supporting Variants
Samples
Known GenesTMEM230
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252627
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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