A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554067



Internal ID16341476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38529438..38659756hg38UCSC Ensembl
Innerchr11:38550988..38681306hg19UCSC Ensembl
Innerchr11:38507564..38637882hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38130319
hg19130319
hg18130319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771149
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554067
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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