A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14383163



Internal ID22281830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66624935..66625423hg38UCSC Ensembl
chr15:66917273..66917761hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218253
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14383163
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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