A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108838



Internal ID21269826
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 StatusS
Merged Variantsnsv3116145
Supporting Variants
Samplessample143
Known GenesALDH9A1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108838
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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