A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4968n223



Internal ID22807936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105454686..105455459hg38UCSC Ensembl
chr3:105173530..105174303hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38774
hg19774
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6570471, nsv6544819
Samples
Known GenesALCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4968n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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