A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222174



Internal ID22366336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80986118..80994523hg38UCSC Ensembl
chr8:81898353..81906758hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg388406
hg198406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341166
SamplesHG00732
Known GenesPAG1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222174
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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