A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363454



Internal ID21021007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20160643..20221178hg38UCSC Ensembl
chr4:20162266..20222801hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3860536
hg1960536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212847
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363454
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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