A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv801n223



Internal ID22803769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69515001..69532900hg38UCSC Ensembl
chr10:71274757..71292656hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3817900
hg1917900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6440897, nsv6437343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv801n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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