A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554408



Internal ID16341817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50360787..50683696hg38UCSC Ensembl
Innerchr11:50319958..50642867hg19UCSC Ensembl
Innerchr11:50276534..50599443hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38322910
hg19322910
hg18322910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1816n54
Supporting Variantsnssv773984
Samples
Known GenesLOC646813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554408
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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