A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553053



Internal ID15993776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1836040..1887776hg38UCSC Ensembl
Innerchr11:1857270..1909006hg19UCSC Ensembl
Innerchr11:1813846..1865582hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3851737
hg1951737
hg1851737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174280
SamplesHGDP00971
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)nsv553053
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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