A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220498



Internal ID22365175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96435573..96435735hg38UCSC Ensembl
chr15:96978803..96978965hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14373378
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220498
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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