A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7846n223



Internal ID22810814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80649101..80667100hg38UCSC Ensembl
chr9:83264016..83282015hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3818000
hg1918000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6446990, nsv6444490, nsv6442081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7846n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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