A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556045



Internal ID16343454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98940429..98965361hg38UCSC Ensembl
Innerchr11:98811159..98836091hg19UCSC Ensembl
Innerchr11:98316369..98341301hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3824933
hg1924933
hg1824933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174923, nssv1174924
SamplesHGDP00003, HGDP01414
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556045
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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