A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6292n223



Internal ID22809260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80801001..80853000hg38UCSC Ensembl
chr6:81510718..81562717hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3852000
hg1952000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6413054, nsv6399538, nsv6410321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6292n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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