A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14371276



Internal ID22228695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39277672..39277755hg38UCSC Ensembl
chr14:39746876..39746959hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528625
Supporting Variants
SamplesHG00733
Known GenesCTAGE5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14371276
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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