A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037711



Internal ID18780242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43202776..43317013hg38UCSC Ensembl
Innerchr13:43776912..43891149hg19UCSC Ensembl
Innerchr13:42674912..42789149hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38114238
hg19114238
hg18114238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1644n100
Supporting Variantsnssv3523422
Samples
Known GenesENOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037711
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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