A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556221



Internal ID16343630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105372644..105521352hg38UCSC Ensembl
Innerchr11:105243371..105392079hg19UCSC Ensembl
Innerchr11:104748581..104897289hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38148709
hg19148709
hg18148709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv783376
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556221
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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