A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155737



Internal ID22086242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31112882..31115659hg38UCSC Ensembl
Outerchr21:31111868..31125413hg38UCSC Ensembl
Innerchr21:32485200..32487977hg19UCSC Ensembl
Outerchr21:32484186..32497731hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3813546
hg1913546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014874
Samples
Known GenesTIAM1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155737
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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