A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116145



Internal ID21299411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165657778..165669584hg38UCSC Ensembl
Innerchr1:165627015..165638821hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3811807
hg1911807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108838, nssv14094987
Samplessample11, sample143
Known GenesALDH9A1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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