A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7779n223



Internal ID22810747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64432101..64470200hg38UCSC Ensembl
chr9:69444519..69482618hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3838100
hg1938100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6452951, nsv6449622, nsv6450369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7779n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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