A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554095



Internal ID16341504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41782613..41797379hg38UCSC Ensembl
Innerchr11:41804163..41818929hg19UCSC Ensembl
Innerchr11:41760739..41775505hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3814767
hg1914767
hg1814767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1759n54
Supporting Variantsnssv771177
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554095
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