A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7828n223



Internal ID22810796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72446419..72448575hg38UCSC Ensembl
chr9:75061335..75063491hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382157
hg192157
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6573624, nsv6565523, nsv6569162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7828n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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