A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214951



Internal ID22361442
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 Variantsnssv14287580
SamplesNA19238
Known GenesCEACAM16
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214951
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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