A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566066



Internal ID16006789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104699427..104714228hg38UCSC Ensembl
Innerchr14:105165764..105180565hg19UCSC Ensembl
Innerchr14:104236809..104251610hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3814802
hg1914802
hg1814802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3955n54
Supporting Variantsnssv834447
Samples
Known GenesINF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566066
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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