A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554184



Internal ID15994907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44886386..44922049hg38UCSC Ensembl
Innerchr11:44907937..44943600hg19UCSC Ensembl
Innerchr11:44864513..44900176hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3835664
hg1935664
hg1835664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv772172
Samples
Known GenesTSPAN18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554184
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