A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7196n223



Internal ID22810164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156264873..156267278hg38UCSC Ensembl
chr7:156057567..156059972hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382406
hg192406
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6422216, nsv6429130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7196n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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