A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518903



Internal ID20892264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29786089..29859796hg38UCSC Ensembl
chr19:30276996..30350703hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3873708
hg1973708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197283
Samples
Known GenesCCNE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518903
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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