A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554065



Internal ID16341474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38331750..38376356hg38UCSC Ensembl
Innerchr11:38353300..38397906hg19UCSC Ensembl
Innerchr11:38309876..38354482hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3844607
hg1944607
hg1844607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771148
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554065
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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