A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14376110



Internal ID22279751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89574198..89574822hg38UCSC Ensembl
chr15:90117429..90118053hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228404
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14376110
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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