A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564073



Internal ID16351482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:25560807..25588489hg38UCSC Ensembl
Innerchr14:26030013..26057695hg19UCSC Ensembl
Innerchr14:25099853..25127535hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3827683
hg1927683
hg1827683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv824519
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564073
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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