A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118145



Internal ID21301411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108863314..109792853hg38UCSC Ensembl
Innerchr3:108582161..109511700hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38929540
hg19929540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103523
Samplessample29
Known GenesDPPA2, DPPA4, FLJ22763, FLJ25363, GUCA1C, LINC00488, MORC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118145
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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