A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448389



Internal ID21105942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132405071..132450604hg38UCSC Ensembl
chr10:134218575..134264108hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3845534
hg1945534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194603
Samples
Known GenesC10orf91, PWWP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448389
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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