A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553830



Internal ID16341239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25020209..25064963hg38UCSC Ensembl
Innerchr11:25041755..25086509hg19UCSC Ensembl
Innerchr11:24998331..25043085hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3844755
hg1944755
hg1844755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1710n54
Supporting Variantsnssv769105
Samples
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553830
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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