A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553819



Internal ID15994542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24477824..24523807hg38UCSC Ensembl
Innerchr11:24499370..24545353hg19UCSC Ensembl
Innerchr11:24455946..24501929hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3845984
hg1945984
hg1845984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv769094
Samples
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553819
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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