A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460803



Internal ID21118356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98002737..98019812hg38UCSC Ensembl
chr12:98396515..98413590hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3817076
hg1917076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460803
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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