A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556431



Internal ID15997154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:108227415..108244860hg38UCSC Ensembl
Innerchr11:108098142..108115587hg19UCSC Ensembl
Innerchr11:107603352..107620797hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3817446
hg1917446
hg1817446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n54
Supporting Variantsnssv784564
Samples
Known GenesATM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556431
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