A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554071



Internal ID16341480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38868581..38987021hg38UCSC Ensembl
Innerchr11:38890131..39008571hg19UCSC Ensembl
Innerchr11:38846707..38965147hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38118441
hg19118441
hg18118441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174637
Samples1780854196_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554071
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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