A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555092



Internal ID16342501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55938897..55962275hg38UCSC Ensembl
Innerchr11:55706373..55729751hg19UCSC Ensembl
Innerchr11:55462949..55486327hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3823379
hg1923379
hg1823379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1947n54
Supporting Variantsnssv1174797
Samples1782681076_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555092
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