A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451662



Internal ID21109215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134845919..135144190hg38UCSC Ensembl
chr9:137737765..138036036hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38298272
hg19298272
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228277
Samples
Known GenesFCN1, FCN2, LOC101448202, MIR3689A, MIR3689B, MIR3689C, MIR3689D1, MIR3689D2, MIR3689E, MIR3689F, OLFM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451662
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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