A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564111



Internal ID16351520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26694881..26893735hg38UCSC Ensembl
Innerchr14:27164087..27362941hg19UCSC Ensembl
Innerchr14:26233927..26432781hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38198855
hg19198855
hg18198855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825054
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564111
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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