A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103523



Internal ID21279857
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 StatusS
Merged Variantsnsv3118145
Supporting Variants
Samplessample29
Known GenesDPPA2, DPPA4, FLJ22763, FLJ25363, GUCA1C, LINC00488, MORC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103523
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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