A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5788n223



Internal ID22808756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74764799..74765725hg38UCSC Ensembl
chr5:74060624..74061550hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6560420, nsv6571222
Samples
Known GenesGFM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5788n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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