A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217017



Internal ID22362819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59537351..59542376hg38UCSC Ensembl
chr8:60449910..60454935hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg385026
hg195026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341582
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217017
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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