A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554425



Internal ID16341834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54784245..55021565hg38UCSC Ensembl
Innerchr11:51095992..51335035hg19UCSC Ensembl
Innerchr11:50952568..51191611hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38237321
hg19239044
hg18239044
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1822n54
Supporting Variantsnssv774014
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554425
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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