A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598741



Internal ID20971812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53633521..53633887hg38UCSC Ensembl
chr20:52250060..52250426hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4491n223
Supporting Variantsnssv18253328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598741
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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