A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565515



Internal ID16006238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89416879..89417204hg38UCSC Ensembl
Innerchr14:89883223..89883548hg19UCSC Ensembl
Innerchr14:88952976..88953301hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38326
hg19326
hg18326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832174
Samples
Known GenesFOXN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565515
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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