A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7627n223



Internal ID22810595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15296601..15397066hg38UCSC Ensembl
chr9:15296599..15397064hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38100466
hg19100466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6419225, nsv6426484
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7627n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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