A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406449



Internal ID21064002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114691401..114849300hg38UCSC Ensembl
chr5:114027098..114184997hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38157900
hg19157900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406449
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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