A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6018n223



Internal ID22808986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165915701..165920200hg38UCSC Ensembl
chr5:165342706..165347205hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6411710, nsv6403452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6018n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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