A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396771



Internal ID21054324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108316569..108337408hg38UCSC Ensembl
chr5:107652270..107673109hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3820840
hg1920840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212727
Samples
Known GenesFBXL17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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