A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5024n223



Internal ID22807992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132678661..132679247hg38UCSC Ensembl
chr3:132397505..132398091hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6559124, nsv6557474
Samples
Known GenesNPHP3-ACAD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5024n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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