A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14369541



Internal ID22289377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59418945..59419687hg38UCSC Ensembl
chr14:59885663..59886405hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214110
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14369541
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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