A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4978n223



Internal ID22807946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111805263..111806936hg38UCSC Ensembl
chr3:111524110..111525783hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg381674
hg191674
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6568758, nsv6564900
Samples
Known GenesPHLDB2, PLCXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4978n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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