A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113307



Internal ID21296573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97080837..97085803hg38UCSC Ensembl
Innerchr8:98093065..98098031hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg384967
hg194967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085314
Samplessample170
Known GenesCPQ
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113307
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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