A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556048



Internal ID16343457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99081487..99112682hg38UCSC Ensembl
Innerchr11:98952217..98983412hg19UCSC Ensembl
Innerchr11:98457427..98488622hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3831196
hg1931196
hg1831196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781720
Samples
Known GenesCNTN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556048
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