A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266406



Internal ID20833446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53776977..53778819hg38UCSC Ensembl
chr4:54643144..54644986hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381843
hg191843
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562976
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266406
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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