A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5077n223



Internal ID22808045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167126101..167132500hg38UCSC Ensembl
chr3:166843889..166850288hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6371958, nsv6364377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5077n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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