A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6423n223



Internal ID22809391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139278601..139296100hg38UCSC Ensembl
chr6:139599738..139617237hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3817500
hg1917500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6603089, nsv6615771
Samples
Known GenesTXLNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6423n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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