A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7626n223



Internal ID22810594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15006946..15159370hg38UCSC Ensembl
chr9:15006944..15159368hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38152425
hg19152425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6430352, nsv6422467
Samples
Known GenesLOC389705
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7626n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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