A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1035n223



Internal ID22804003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45400769..45414878hg38UCSC Ensembl
chr11:45422319..45436428hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3814110
hg1914110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6466491, nsv6459049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1035n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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