A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556014



Internal ID16343423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97962449..98044598hg38UCSC Ensembl
Innerchr11:97833177..97915326hg19UCSC Ensembl
Innerchr11:97338387..97420536hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3882150
hg1982150
hg1882150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2108n54
Supporting Variantsnssv781689
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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