A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253472



Internal ID20820512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11274013..11311081hg38UCSC Ensembl
chr20:11254661..11291729hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3837069
hg1937069
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253472
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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