A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389693



Internal ID21047246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14025840..14026168hg38UCSC Ensembl
chr5:14025949..14026277hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389693
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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