A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv974n223



Internal ID22803942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9622101..9623600hg38UCSC Ensembl
chr11:9643648..9645147hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6447737, nsv6446385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv974n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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