A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7533n223



Internal ID22810501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:44061..452686hg38UCSC Ensembl
chr9:44061..452686hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38408626
hg19408626
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6431769, nsv6433848, nsv6428594, nsv6419331, nsv6426195
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7533n223
Frequency
Sample Size19652
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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