A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526536



Internal ID15107143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28322483..30669172hg38UCSC Ensembl
Innerchr14:28791689..31138378hg19UCSC Ensembl
Innerchr14:27861440..30208129hg18UCSC Ensembl
Innerchr14:27861440..30208129hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382346690
hg192346690
hg182346690
hg172346690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702849
Samples
Known GenesC14orf23, FOXG1, G2E3, MIR548AI, PRKD1, SCFD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526536
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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