A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553925



Internal ID16341334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28985831..29015092hg38UCSC Ensembl
Innerchr11:29007378..29036639hg19UCSC Ensembl
Innerchr11:28963954..28993215hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3829262
hg1929262
hg1829262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv770280
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553925
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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