A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556278



Internal ID16343687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107087578..107136174hg38UCSC Ensembl
Innerchr11:106958304..107006900hg19UCSC Ensembl
Innerchr11:106463514..106512110hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3848597
hg1948597
hg1848597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv783725
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556278
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