A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2586n223



Internal ID22805554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75629740..75644207hg38UCSC Ensembl
chr15:75922081..75936548hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3814468
hg1914468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6511860, nsv6505197
Samples
Known GenesIMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2586n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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