A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376171



Internal ID21033724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25461269..25502971hg38UCSC Ensembl
chr5:25461378..25503080hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3841703
hg1941703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376171
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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