A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553454



Internal ID15994177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9037645..9103754hg38UCSC Ensembl
Innerchr11:9059192..9125301hg19UCSC Ensembl
Innerchr11:9015768..9081877hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3866110
hg1966110
hg1866110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767062
Samples
Known GenesKRT8P41, MIR5691, SCUBE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553454
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