A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213357



Internal ID22360328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68825360..68825645hg38UCSC Ensembl
chr15:69117699..69117984hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387615, nssv14379922
SamplesHG00512, HG00513
Known GenesMIR548H4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213357
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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