A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554417



Internal ID16341826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:50504005..50791553hg38UCSC Ensembl
Innerchr11:50463176..50750724hg19UCSC Ensembl
Innerchr11:50419752..50707300hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38287549
hg19287549
hg18287549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1820n54
Supporting Variantsnssv774007
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554417
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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