A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555669



Internal ID16343078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86571638..86575548hg38UCSC Ensembl
Innerchr11:86282680..86286590hg19UCSC Ensembl
Innerchr11:85960328..85964238hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383911
hg193911
hg183911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2046n54
Supporting Variantsnssv779966
Samples
Known GenesME3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555669
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