A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221718



Internal ID22366005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9640323..9643446hg38UCSC Ensembl
chr8:9497833..9500956hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383124
hg193124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341428, nssv14341427
SamplesNA19238, NA19240
Known GenesTNKS
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221718
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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