A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564159



Internal ID16351568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28728997..28738995hg38UCSC Ensembl
Innerchr14:29198203..29208201hg19UCSC Ensembl
Innerchr14:28267954..28277952hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg389999
hg199999
hg189999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3603n54
Supporting Variantsnssv825109
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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