A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453942



Internal ID21111495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131446996..131946727hg38UCSC Ensembl
chr10:133245259..133760231hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38499732
hg19514973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv915n223
Supporting Variantsnssv18181065
Samples
Known GenesFLJ46300, PPP2R2D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453942
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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