A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554097



Internal ID16341506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41782617..41797430hg38UCSC Ensembl
Innerchr11:41804167..41818980hg19UCSC Ensembl
Innerchr11:41760743..41775556hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3814814
hg1914814
hg1814814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1759n54
Supporting Variantsnssv771179
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554097
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