A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4951n223



Internal ID22807919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99401745..99402760hg38UCSC Ensembl
chr3:99120589..99121604hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6554725, nsv6539427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4951n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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