A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7720n223



Internal ID22810688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41049801..41142900hg38UCSC Ensembl
chr9:70903339..70986000hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3893100
hg1982662
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6436428, nsv6442903, nsv6447639, nsv6454051, nsv6450978, nsv6443882
Samples
Known GenesCBWD3, FOXD4L3, PGM5, PGM5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7720n223
Frequency
Sample Size19652
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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