A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14371302



Internal ID22228721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39697431..39699755hg38UCSC Ensembl
chr14:40166635..40168959hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382325
hg192325
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227204
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14371302
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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