A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403854



Internal ID21061407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151589614..151593045hg38UCSC Ensembl
chr5:150969175..150972606hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383432
hg193432
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403854
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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