A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566160



Internal ID16006883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105151554..105219528hg38UCSC Ensembl
Innerchr14:105617891..105685865hg19UCSC Ensembl
Innerchr14:104688936..104756910hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3867975
hg1967975
hg1867975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3977n54
Supporting Variantsnssv834736
Samples
Known GenesBRF1, JAG2, NUDT14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566160
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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