A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553781



Internal ID16341190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24088370..24201455hg38UCSC Ensembl
Innerchr11:24109916..24223001hg19UCSC Ensembl
Innerchr11:24066492..24179577hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38113086
hg19113086
hg18113086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1700n54
Supporting Variantsnssv768977
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553781
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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