A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213046



Internal ID22360116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97447171..97447380hg38UCSC Ensembl
chr8:98459399..98459608hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342065, nssv14342064, nssv14342063
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213046
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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