A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5056n223



Internal ID22808024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155573927..155575004hg38UCSC Ensembl
chr3:155291716..155292793hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381078
hg191078
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6560470, nsv6572183
Samples
Known GenesPLCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5056n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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