A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252611



Internal ID20819651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5075106..5075584hg38UCSC Ensembl
chr20:5055752..5056230hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599392
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252611
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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