A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566030



Internal ID16006753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104088584..104164374hg38UCSC Ensembl
Innerchr14:104554921..104630711hg19UCSC Ensembl
Innerchr14:103624674..103700464hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3875791
hg1975791
hg1875791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834415
Samples
Known GenesASPG, KIF26A, MIR203, MIR3545
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566030
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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