A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553294



Internal ID16340703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5739717..5741056hg38UCSC Ensembl
Innerchr11:5760947..5762286hg19UCSC Ensembl
Innerchr11:5717523..5718862hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381340
hg191340
hg181340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv765887
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553294
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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