A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566229



Internal ID16353638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474172..105483783hg38UCSC Ensembl
Innerchr14:105940509..105950120hg19UCSC Ensembl
Innerchr14:105011554..105021165hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg389612
hg199612
hg189612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834843
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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