A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253421



Internal ID20820461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5761706..5762083hg38UCSC Ensembl
chr20:5742352..5742729hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598941
Supporting Variants
Samples
Known GenesC20orf196
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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