A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223774



Internal ID22367447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98634273..98634434hg38UCSC Ensembl
chr15:99177502..99177663hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375000, nssv14389754
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223774
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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