A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14374170



Internal ID22207510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60516173..60516237hg38UCSC Ensembl
chr15:60808372..60808436hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211449
Supporting Variants
SamplesHG00732
Known GenesRORA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14374170
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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