A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5849n223



Internal ID22808817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102670801..102677600hg38UCSC Ensembl
chr5:102006505..102013304hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6410891, nsv6396021, nsv6407164
Samples
Known GenesLINC00491
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5849n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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