A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117034



Internal ID21300300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19018903..19023871hg38UCSC Ensembl
Innerchr21:20391222..20396190hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg384969
hg194969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102003
Samplessample194
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117034
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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