A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7532n223



Internal ID22810500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42223..258649hg38UCSC Ensembl
chr9:42223..258649hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38216427
hg19216427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6426659, nsv6435466
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7532n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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