A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247025



Internal ID20814065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144077918..144883948hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38806031
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247025
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00031


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