A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554078



Internal ID16341487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39053004..39119483hg38UCSC Ensembl
Innerchr11:39074554..39141033hg19UCSC Ensembl
Innerchr11:39031130..39097609hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3866480
hg1966480
hg1866480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1757n54
Supporting Variantsnssv771161
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554078
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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