A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210984



Internal ID22358693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28198588..28198701hg38UCSC Ensembl
chr8:28056105..28056218hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14339703
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210984
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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