A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047876



Internal ID18790407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:25055911..25162386hg38UCSC Ensembl
Innerchr13:25630049..25736524hg19UCSC Ensembl
Innerchr13:24528049..24634524hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38106476
hg19106476
hg18106476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523204
Samples
Known GenesPABPC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047876
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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