A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403898



Internal ID21061451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66792991..67132623hg38UCSC Ensembl
chr5:66088819..66428451hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38339633
hg19339633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214849
Samples
Known GenesMAST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403898
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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