A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520282



Internal ID8414557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28755627..28774515hg38UCSC Ensembl
Innerchr14:29224833..29243721hg19UCSC Ensembl
Innerchr14:28294584..28313472hg18UCSC Ensembl
Innerchr14:28294584..28313472hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3818889
hg1918889
hg1818889
hg1718889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697324
Samples
Known GenesC14orf23, FOXG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520282
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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