A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393188



Internal ID21050741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17829451..17842701hg38UCSC Ensembl
chr5:17829560..17842810hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3813251
hg1913251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393188
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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