A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7954n223



Internal ID22810922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133060690..133082200hg38UCSC Ensembl
chr9:135936077..135957587hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3821511
hg1921511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6441705, nsv6452857, nsv6448899
Samples
Known GenesCEL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7954n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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