A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv767789



Internal ID16061745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9998332..10038076hg38UCSC Ensembl
Innerchr11:10019879..10059623hg19UCSC Ensembl
Innerchr11:9976455..10016199hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3839745
hg1939745
hg1839745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553475
Supporting Variants
Samples
Known GenesSBF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv767789
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