A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554026



Internal ID16341435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38109249..38300656hg38UCSC Ensembl
Innerchr11:38130799..38322206hg19UCSC Ensembl
Innerchr11:38087375..38278782hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38191408
hg19191408
hg18191408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1748n54
Supporting Variantsnssv1174623
SamplesNINDS_103
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554026
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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