A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452349



Internal ID21109902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89296729..89438494hg38UCSC Ensembl
chr9:91911644..92053409hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38141766
hg19141766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233991
Samples
Known GenesCKS2, MIR3153, SECISBP2, SEMA4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452349
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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