A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566020



Internal ID16353429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103522942..103530059hg38UCSC Ensembl
Innerchr14:103989279..103996396hg19UCSC Ensembl
Innerchr14:103059032..103066149hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg387118
hg197118
hg187118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834396, nssv834395, nssv834394
Samples
Known GenesTRMT61A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566020
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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