A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7955n223



Internal ID22810923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133060701..133068000hg38UCSC Ensembl
chr9:135936088..135943387hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6454528, nsv6451474
Samples
Known GenesCEL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7955n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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