A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554596



Internal ID16342005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54525403..54537349hg38UCSC Ensembl
Innerchr11:51581931..51593877hg19UCSC Ensembl
Innerchr11:51438507..51450453hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg3811947
hg1911947
hg1811947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv774656, nssv774655, nssv774657
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554596
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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