A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114022



Internal ID21297288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196787125..196926784hg38UCSC Ensembl
Innerchr1:196756255..196895914hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38139660
hg19139660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv102n145
Supporting Variantsnssv14083083
Samplessample174
Known GenesCFHR1, CFHR3, CFHR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114022
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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