A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4588n223



Internal ID22807556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31727226..31727744hg38UCSC Ensembl
chr21:33099539..33100057hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6599885, nsv6595838
Samples
Known GenesSCAF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4588n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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