A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556009



Internal ID16343418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97686786..97746563hg38UCSC Ensembl
Innerchr11:97557786..97617563hg19UCSC Ensembl
Innerchr11:97062996..97122773hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3859778
hg1959778
hg1859778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174914
SamplesHGDP00716
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556009
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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