A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253329



Internal ID20820369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53633598..53633993hg38UCSC Ensembl
chr20:52250137..52250532hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253329
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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