A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3558111



Internal ID22426914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41803742..41807380hg38UCSC Ensembl
chr19:42307806..42311418hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383639
hg193613
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286873, nssv14286871, nssv14286870, nssv14286869, nssv14286868, nssv14286872
SamplesHG00512, HG00731, HG00732, HG00733, HG00513, HG00514
Known GenesCEACAM3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3558111
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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