A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5349n223



Internal ID22808317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84865035..84866050hg38UCSC Ensembl
chr4:85786188..85787203hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg381016
hg191016
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6572175, nsv6570421
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5349n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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