A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7018n223



Internal ID22809986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97758901..97779100hg38UCSC Ensembl
chr7:97388213..97408412hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3820200
hg1920200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6611251, nsv6609177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7018n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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