A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554011



Internal ID16341420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37673660..37810072hg38UCSC Ensembl
Innerchr11:37695210..37831622hg19UCSC Ensembl
Innerchr11:37651786..37788198hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38136413
hg19136413
hg18136413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1744n54
Supporting Variantsnssv771068
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554011
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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