A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450479



Internal ID21108032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13580085..13654761hg38UCSC Ensembl
chr10:13622085..13696761hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3874677
hg1974677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196536
Samples
Known GenesFRMD4A, PRPF18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450479
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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