A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565706



Internal ID16006429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99156693..99190855hg38UCSC Ensembl
Innerchr14:99623030..99657192hg19UCSC Ensembl
Innerchr14:98692783..98726945hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3834163
hg1934163
hg1834163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832934
Samples
Known GenesBCL11B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565706
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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