A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587741



Internal ID16028464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44248288..44263467hg38UCSC Ensembl
Innerchr21:45668171..45683350hg19UCSC Ensembl
Innerchr21:44492599..44507778hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3815180
hg1915180
hg1815180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948224
Samples
Known GenesDNMT3L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587741
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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