A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155738



Internal ID22086243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38742218..38782388hg38UCSC Ensembl
Outerchr21:38732522..38783137hg38UCSC Ensembl
Innerchr21:40114142..40154312hg19UCSC Ensembl
Outerchr21:40104446..40155061hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3850616
hg1950616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014875
Samples
Known GenesLINC00114
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155738
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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