A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598799



Internal ID20971870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21409821..21440249hg38UCSC Ensembl
chr20:21390459..21420887hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3830429
hg1930429
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253655
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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