A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100923



Internal ID21291727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38814837..38817243hg38UCSC Ensembl
Innerchr21:40186761..40189167hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg382407
hg192407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112905
Supporting Variants
Samplessample78
Known GenesETS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100923
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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