A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14382548



Internal ID22267713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68133672..68136589hg38UCSC Ensembl
chr15:68426010..68428927hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382918
hg192918
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529123
Supporting Variants
SamplesNA19238
Known GenesPIAS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14382548
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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