A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556559



Internal ID16343968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128789592..128799925hg38UCSC Ensembl
Innerchr11:128659487..128669820hg19UCSC Ensembl
Innerchr11:128164697..128175030hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3810334
hg1910334
hg1810334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175755
SamplesHGDP01077
Known GenesFLI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556559
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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