A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556562



Internal ID16343971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128812855..128817410hg38UCSC Ensembl
Innerchr11:128682750..128687305hg19UCSC Ensembl
Innerchr11:128187960..128192515hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg384556
hg194556
hg184556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785099
Samples
Known GenesFLI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556562
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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