A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410147



Internal ID21067700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165604642..165646355hg38UCSC Ensembl
chr5:165031647..165073360hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3841714
hg1941714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410147
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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