A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110485



Internal ID21293751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196825272..196926860hg38UCSC Ensembl
Innerchr1:196794402..196895990hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38101589
hg19101589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv102n145
Supporting Variantsnssv14102839, nssv14085981
Samplessample41, sample21
Known GenesCFHR1, CFHR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110485
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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