A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252286



Internal ID20819326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27736946..27737724hg38UCSC Ensembl
chr1:28063457..28064235hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38779
hg19779
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554025
Supporting Variants
Samples
Known GenesFAM76A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252286
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00039


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