A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553823



Internal ID16341232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24756565..24767131hg38UCSC Ensembl
Innerchr11:24778111..24788677hg19UCSC Ensembl
Innerchr11:24734687..24745253hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3810567
hg1910567
hg1810567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1709n54
Supporting Variantsnssv769098, nssv769097
Samples
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553823
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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