A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14285242



Internal ID22296941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7688879..7688943hg38UCSC Ensembl
chr19:7753765..7753829hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223235
Supporting Variants
SamplesNA19240
Known GenesFCER2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14285242
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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