A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598892



Internal ID20971963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44515174..44515854hg38UCSC Ensembl
chr20:43143815..43144495hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38681
hg19681
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252103
Samples
Known GenesSERINC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598892
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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