A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5892n223



Internal ID22808860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112278229..112279073hg38UCSC Ensembl
chr5:111613926..111614770hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6567114, nsv6560124
Samples
Known GenesEPB41L4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5892n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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