A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4914n223



Internal ID22807882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75273401..75811700hg38UCSC Ensembl
chr3:75322552..75860851hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38538300
hg19538300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6372692, nsv6369575
Samples
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4914n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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