A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566264



Internal ID16353673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474766..105477662hg38UCSC Ensembl
Innerchr14:105941103..105943999hg19UCSC Ensembl
Innerchr14:105012148..105015044hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg382897
hg192897
hg182897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3994n54
Supporting Variantsnssv834929
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566264
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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