A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224381



Internal ID22367831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95079877..95080118hg38UCSC Ensembl
chr8:96092105..96092346hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9258n152
Supporting Variantsnssv14342818, nssv14342819, nssv14342817
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224381
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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