A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113565



Internal ID21296831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166576409..166646783hg38UCSC Ensembl
Innerchr1:166545646..166616020hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3870375
hg1970375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091098, nssv14083429, nssv14104563
Samplessample271, sample189, sample48
Known GenesFMO9P
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113565
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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