A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553146



Internal ID15993869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3653813..3655845hg38UCSC Ensembl
Innerchr11:3675043..3677075hg19UCSC Ensembl
Innerchr11:3631619..3633651hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382033
hg192033
hg182033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1581n54
Supporting Variantsnssv764632
Samples
Known GenesART1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553146
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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