A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555636



Internal ID16343045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85720843..85754136hg38UCSC Ensembl
Innerchr11:85431886..85465179hg19UCSC Ensembl
Innerchr11:85109534..85142827hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3833294
hg1933294
hg1833294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2040n54
Supporting Variantsnssv779878
Samples
Known GenesSYTL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555636
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer