A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226043



Internal ID22368986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91304256..91304326hg38UCSC Ensembl
chr15:91847486..91847556hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375002
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226043
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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