A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566031



Internal ID16353440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104088984..104114735hg38UCSC Ensembl
Innerchr14:104555321..104581072hg19UCSC Ensembl
Innerchr14:103625074..103650825hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3825752
hg1925752
hg1825752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834416
Samples
Known GenesASPG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566031
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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