A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460838



Internal ID21118391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90557352..90819825hg38UCSC Ensembl
chr12:90951129..91213602hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38262474
hg19262474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460838
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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