A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597493



Internal ID20970564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45847537..45848132hg38UCSC Ensembl
chr20:44476176..44476771hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252134
Samples
Known GenesACOT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597493
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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