A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1929n209



Internal ID22828004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142773050..142774865hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381816
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5852107, nsv5864511
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1929n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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