A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7886n223



Internal ID22810854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96846901..96861500hg38UCSC Ensembl
chr9:99609183..99623782hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3814600
hg1914600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6448536, nsv6445691
Samples
Known GenesZNF782
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7886n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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