A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036311



Internal ID18778842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:42970143..43139457hg38UCSC Ensembl
Innerchr13:43544279..43713593hg19UCSC Ensembl
Innerchr13:42442279..42611593hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38169315
hg19169315
hg18169315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1641n100
Supporting Variantsnssv3714974
Samples
Known GenesDNAJC15, EPSTI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036311
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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