A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599945



Internal ID20973016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21181615..21182515hg38UCSC Ensembl
chr20:21162255..21163155hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253650
Samples
Known GenesPLK1S1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599945
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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