A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5526n223



Internal ID22808494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157146169..157146825hg38UCSC Ensembl
chr4:158067321..158067977hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6570162, nsv6575328
Samples
Known GenesGLRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5526n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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