A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220872



Internal ID22365443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102854021..102854556hg38UCSC Ensembl
chr8:103866249..103866784hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342206, nssv14342207
SamplesNA19238, HG00733
Known GenesAZIN1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220872
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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