A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037828



Internal ID18780359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:114219408..114342910hg38UCSC Ensembl
Innerchr13:114984883..115108385hg19UCSC Ensembl
Innerchr13:114002985..114126487hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38123503
hg19123503
hg18123503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1746n100
Supporting Variantsnssv3525656
Samples
Known GenesCDC16, CHAMP1, UPF3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037828
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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