A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451878



Internal ID21109431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124783333..124804948hg38UCSC Ensembl
chr10:126471902..126493517hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3821616
hg1921616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183923
Samples
Known GenesFAM175B, METTL10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451878
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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