A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399008



Internal ID21056561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14221446..14238322hg38UCSC Ensembl
chr6:14221677..14238553hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3816877
hg1916877
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216916
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399008
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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