A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555635



Internal ID16343044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85719354..85759850hg38UCSC Ensembl
Innerchr11:85430397..85470893hg19UCSC Ensembl
Innerchr11:85108045..85148541hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3840497
hg1940497
hg1840497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2040n54
Supporting Variantsnssv779875, nssv779876, nssv779877
Samples
Known GenesSYTL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555635
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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