A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv699n223



Internal ID22803667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41774701..41856000hg38UCSC Ensembl
chr10:42384209..42465508hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3881300
hg1981300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6454747, nsv6437406, nsv6449407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv699n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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