A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14387222



Internal ID22274735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72209407..72209459hg38UCSC Ensembl
chr15:72501748..72501800hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529538
Supporting Variants
SamplesNA19239
Known GenesPKM
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14387222
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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