A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370372



Internal ID22147630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65363265..65363319hg38UCSC Ensembl
chr14:65829983..65830037hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211229
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370372
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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