A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115943



Internal ID21299209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88385406..88390736hg38UCSC Ensembl
Innerchr9:91000321..91005651hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg385331
hg195331
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088121
Samplessample345
Known GenesSPIN1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115943
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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