A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363478



Internal ID21021031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55160836..55214043hg38UCSC Ensembl
chr3:55194864..55248071hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3853208
hg1953208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363478
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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