A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423791



Internal ID21081344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63160301..63183800hg38UCSC Ensembl
chr8:64072860..64096359hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3823500
hg1923500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235970
Samples
Known GenesYTHDF3, YTHDF3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423791
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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