A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6002n223



Internal ID22808970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157586774..157587632hg38UCSC Ensembl
chr5:157013782..157014640hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6573150, nsv6555960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6002n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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