A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4422n223



Internal ID22807390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18146429..18147628hg38UCSC Ensembl
chr20:18127073..18128272hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6597764, nsv6596481
Samples
Known GenesCSRP2BP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4422n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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