A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5206n223



Internal ID22808174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25187953..25188717hg38UCSC Ensembl
chr4:25189575..25190339hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6571136, nsv6570216
Samples
Known GenesSEPSECS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5206n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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