A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2991n223



Internal ID22805959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6853147..6972729hg38UCSC Ensembl
chr17:6756466..6876048hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38119583
hg19119583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6501883, nsv6513786
Samples
Known GenesALOX12P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2991n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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