A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764472



Internal ID15711742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1844330..1883298hg38UCSC Ensembl
Innerchr11:1865560..1904528hg19UCSC Ensembl
Innerchr11:1822136..1861104hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3838969
hg1938969
hg1838969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553056
Supporting Variants
Samples
Known GenesLSP1, MIR4298
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764472
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