A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7639n223



Internal ID22810607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19375227..19491739hg38UCSC Ensembl
chr9:19375225..19491737hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38116513
hg19116513
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6426620, nsv6435157
Samples
Known GenesACER2, RPS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7639n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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