A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv765880



Internal ID16059836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5738876..5741619hg38UCSC Ensembl
Innerchr11:5760106..5762849hg19UCSC Ensembl
Innerchr11:5716682..5719425hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382744
hg192744
hg182744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553287
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv765880
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