A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564836



Internal ID16352245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:50138853..50160118hg38UCSC Ensembl
Innerchr14:50605571..50626836hg19UCSC Ensembl
Innerchr14:49675321..49696586hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3821266
hg1921266
hg1821266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827868
Samples
Known GenesSOS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564836
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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