A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565029



Internal ID16352438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70221635..70222673hg38UCSC Ensembl
Innerchr14:70688352..70689390hg19UCSC Ensembl
Innerchr14:69758105..69759143hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381039
hg191039
hg181039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3748n54
Supporting Variantsnssv829035, nssv829034, nssv829041, nssv829032, nssv829036, nssv829037, nssv829042, nssv829038, nssv829044, nssv829033, nssv829046, nssv829045, nssv829043, nssv829040, nssv829039
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565029
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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