A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3329n223



Internal ID22806297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24288761..24289422hg38UCSC Ensembl
chr18:21868725..21869386hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6591270, nsv6585354
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3329n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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