A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368463



Internal ID21026016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22887336..22891688hg38UCSC Ensembl
chr4:22888959..22893311hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384353
hg194353
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368463
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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