A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115461



Internal ID21298727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:219696378..219699951hg38UCSC Ensembl
Innerchr1:219869720..219873293hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383574
hg193574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv113n145
Supporting Variantsnssv14091362, nssv14086753
Samplessample206, sample299
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115461
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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