A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450708



Internal ID21108261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13114133..13146145hg38UCSC Ensembl
chr10:13156133..13188145hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3832013
hg1932013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182727
Samples
Known GenesOPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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