A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553821



Internal ID16341230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24725391..24753967hg38UCSC Ensembl
Innerchr11:24746937..24775513hg19UCSC Ensembl
Innerchr11:24703513..24732089hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3828577
hg1928577
hg1828577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv769096
Samples
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553821
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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