A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553728



Internal ID16341137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22015025..22134911hg38UCSC Ensembl
Innerchr11:22036571..22156457hg19UCSC Ensembl
Innerchr11:21993147..22113033hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38119887
hg19119887
hg18119887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768866
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553728
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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