A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488418



Internal ID21145971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110699901..110714900hg38UCSC Ensembl
chr12:111137706..111152705hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3815000
hg1915000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488418
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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