A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553997



Internal ID15994720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34436683..34439164hg38UCSC Ensembl
Innerchr11:34458230..34460711hg19UCSC Ensembl
Innerchr11:34414806..34417287hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382482
hg192482
hg182482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771054
Samples
Known GenesCAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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