A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7572n223



Internal ID22810540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11647634..12011399hg38UCSC Ensembl
chr9:11647634..12011399hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38363766
hg19363766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6431194, nsv6423386, nsv6432557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7572n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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