A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6619n223



Internal ID22809587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23367176..23367718hg38UCSC Ensembl
chr7:23406795..23407337hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6557693, nsv6555872
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6619n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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