A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555770



Internal ID15996493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89496263..89733564hg38UCSC Ensembl
Innerchr11:89229431..89466732hg19UCSC Ensembl
Innerchr11:88869079..89106380hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38237302
hg19237302
hg18237302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175390
SamplesHGDP00804
Known GenesFOLH1B, NOX4, TRIM77
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555770
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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