A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4969n223



Internal ID22807937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106433824..106435235hg38UCSC Ensembl
chr3:106152671..106154082hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg381412
hg191412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6568154, nsv6571247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4969n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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