A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376391



Internal ID21033944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28737413..28744528hg38UCSC Ensembl
chr5:28737520..28744635hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg387116
hg197116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376391
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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