A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552768



Internal ID16340177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:319882..356090hg38UCSC Ensembl
Innerchr11:319882..356090hg19UCSC Ensembl
Innerchr11:309882..346090hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3836209
hg1936209
hg1836209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763051
Samples
Known GenesIFITM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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