A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565514



Internal ID16006237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89416879..89416981hg38UCSC Ensembl
Innerchr14:89883223..89883325hg19UCSC Ensembl
Innerchr14:88952976..88953078hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38103
hg19103
hg18103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832173
Samples
Known GenesFOXN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565514
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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