A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598476



Internal ID20971547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21207770..21208636hg38UCSC Ensembl
chr20:21188408..21189274hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253651
Samples
Known GenesPLK1S1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598476
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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