A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398395



Internal ID21055948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155265681..155265997hg38UCSC Ensembl
chr5:154645241..154645557hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398395
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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