A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14308437



Internal ID22265415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111425955..111430897hg38UCSC Ensembl
chr3:111144802..111149744hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg384943
hg194943
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201569
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14308437
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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