A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596962



Internal ID20970033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22685082..22692451hg38UCSC Ensembl
chr20:22665720..22673089hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg387370
hg197370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596962
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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