A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252837



Internal ID20819877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1024850..1026582hg38UCSC Ensembl
chr20:1005493..1007225hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381733
hg191733
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252837
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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