A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566449



Internal ID16353858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105738861..105739729hg38UCSC Ensembl
Innerchr14:106205198..106206066hg19UCSC Ensembl
Innerchr14:105276243..105277111hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38869
hg19869
hg18869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4035n54
Supporting Variantsnssv835286
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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