A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6445n223



Internal ID22809413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145725401..145741600hg38UCSC Ensembl
chr6:146046537..146062736hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3816200
hg1916200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6604202, nsv6601749
Samples
Known GenesEPM2A, LOC100507557
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6445n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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