A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv825056



Internal ID16119012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26944801..26997939hg38UCSC Ensembl
Innerchr14:27414007..27467145hg19UCSC Ensembl
Innerchr14:26483847..26536985hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3853139
hg1953139
hg1853139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564113
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)nssv825056
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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