A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554865



Internal ID15995588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602849..55634231hg38UCSC Ensembl
Innerchr11:55370325..55401707hg19UCSC Ensembl
Innerchr11:55126901..55158283hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3831383
hg1931383
hg1831383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1910n54
Supporting Variantsnssv775926
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554865
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