A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117827



Internal ID21301093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:25372689..25374005hg38UCSC Ensembl
Innerchr21:26745003..26746319hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg381317
hg191317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100946
Samplessample96
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117827
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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