A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14309487



Internal ID22274246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139013406..139013697hg38UCSC Ensembl
chr3:138732248..138732539hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191786
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14309487
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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