A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553547



Internal ID15994270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12277374..12318958hg38UCSC Ensembl
Innerchr11:12298921..12340505hg19UCSC Ensembl
Innerchr11:12255497..12297081hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3841585
hg1941585
hg1841585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768249
Samples
Known GenesMICALCL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553547
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