A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564149



Internal ID16351558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28087101..28144861hg38UCSC Ensembl
Innerchr14:28556307..28614067hg19UCSC Ensembl
Innerchr14:27626058..27683818hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3857761
hg1957761
hg1857761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3600n54
Supporting Variantsnssv825089
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564149
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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