A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv826659



Internal ID16120615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40385828..40470194hg38UCSC Ensembl
Innerchr14:40855032..40939398hg19UCSC Ensembl
Innerchr14:39924782..40009148hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3884367
hg1984367
hg1884367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564457
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv826659
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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