A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565707



Internal ID16006430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99166653..99175671hg38UCSC Ensembl
Innerchr14:99632990..99642008hg19UCSC Ensembl
Innerchr14:98702743..98711761hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg389019
hg199019
hg189019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832935
Samples
Known GenesBCL11B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565707
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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