A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215619



Internal ID22361887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31621731..31631053hg38UCSC Ensembl
chr15:31913934..31923256hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg389323
hg199323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14385243
SamplesHG00732
Known GenesOTUD7A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215619
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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