A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565456



Internal ID16352865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85983020..86021785hg38UCSC Ensembl
Innerchr14:86449364..86488129hg19UCSC Ensembl
Innerchr14:85519117..85557882hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3838766
hg1938766
hg1838766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3832n54
Supporting Variantsnssv832012
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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