A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566021



Internal ID16353430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103523302..103546645hg38UCSC Ensembl
Innerchr14:103989639..104012982hg19UCSC Ensembl
Innerchr14:103059392..103082735hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3823344
hg1923344
hg1823344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834397
Samples
Known GenesTRMT61A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566021
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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