A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218859



Internal ID22364073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51953585..51954008hg38UCSC Ensembl
chr15:52245782..52246205hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14389858
SamplesHG00732
Known GenesLEO1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218859
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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