A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555625



Internal ID16343034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84836398..84917969hg38UCSC Ensembl
Innerchr11:84547441..84629013hg19UCSC Ensembl
Innerchr11:84225089..84306661hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3881572
hg1981573
hg1881573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779864
Samples
Known GenesDLG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555625
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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