A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1928n209



Internal ID22828003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142747768..142774543hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3826776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5924118, nsv5914842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1928n209
Frequency
Sample Size914
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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