A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553829



Internal ID16341238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25020209..25061277hg38UCSC Ensembl
Innerchr11:25041755..25082823hg19UCSC Ensembl
Innerchr11:24998331..25039399hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3841069
hg1941069
hg1841069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1710n54
Supporting Variantsnssv769104
Samples
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553829
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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