A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113015



Internal ID21296281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:39982273..39984607hg38UCSC Ensembl
Innerchr21:41354200..41356534hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg382335
hg192335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100860
Samplessample12
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113015
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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