A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415234



Internal ID21072787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98637460..98646005hg38UCSC Ensembl
chr5:97973164..97981709hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg388546
hg198546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415234
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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