A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv976n209



Internal ID22827051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70375891..70381882hg38UCSC Ensembl
chr18:68043127..68049118hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg385992
hg195992
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5872070, nsv5869113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv976n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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