A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554022



Internal ID16341431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37929110..37985098hg38UCSC Ensembl
Innerchr11:37950660..38006648hg19UCSC Ensembl
Innerchr11:37907236..37963224hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3855989
hg1955989
hg1855989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1747n54
Supporting Variantsnssv1174622
Samples1798860114_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554022
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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