A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525495



Internal ID20898856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44709109..44709928hg38UCSC Ensembl
chr19:45212381..45213200hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198850
Samples
Known GenesCEACAM16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525495
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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