A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406837



Internal ID21064390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145689985..145696155hg38UCSC Ensembl
chr5:145069548..145075718hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386171
hg196171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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