A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465114



Internal ID21122667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90882995..90923535hg38UCSC Ensembl
chr12:91276772..91317312hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3840541
hg1940541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187938
Samples
Known GenesLINC00615
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465114
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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