A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564418



Internal ID16351827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39488233..39627684hg38UCSC Ensembl
Innerchr14:39957437..40096888hg19UCSC Ensembl
Innerchr14:39027188..39166639hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38139452
hg19139452
hg18139452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148953
SamplesHGDP00563
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564418
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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