A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198849



Internal ID20765889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44670834..44679343hg38UCSC Ensembl
chr19:45174106..45182615hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg388510
hg198510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525804
Supporting Variants
Samples
Known GenesCEACAM19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198849
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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