A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450037



Internal ID21107590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78018043..78052789hg38UCSC Ensembl
chr10:79777801..79812547hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3834747
hg1934747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188361
Samples
Known GenesPOLR3A, RPS24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450037
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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