A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380285



Internal ID21037838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40109430..40113564hg38UCSC Ensembl
chr5:40109532..40113666hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg384135
hg194135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380285
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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