A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448287



Internal ID21105840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67580034..67672307hg38UCSC Ensembl
chr10:69339792..69432065hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3892274
hg1992274
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179141
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448287
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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