A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7746n223



Internal ID22810714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41767301..41910400hg38UCSC Ensembl
chr9:65645562..67676225hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38143100
hg192030664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6436008, nsv6448220, nsv6444245
Samples
Known GenesAQP7P1, LOC286297, PTGER4P2-CDK2AP2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7746n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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