A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553050



Internal ID15993773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1813024..1884944hg38UCSC Ensembl
Innerchr11:1834254..1906174hg19UCSC Ensembl
Innerchr11:1790830..1862750hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3871921
hg1971921
hg1871921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764467
Samples
Known GenesLSP1, MIR4298, SYT8, TNNI2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553050
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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