A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459089



Internal ID21116642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80079156..80082605hg38UCSC Ensembl
chr12:80472936..80476385hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg383450
hg193450
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185781
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459089
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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