A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036563



Internal ID18779094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:42970143..43155032hg38UCSC Ensembl
Innerchr13:43544279..43729168hg19UCSC Ensembl
Innerchr13:42442279..42627168hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38184890
hg19184890
hg18184890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1641n100
Supporting Variantsnssv3523411, nssv3523410
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)nsv1036563
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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