A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112905



Internal ID21296171
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 StatusM
Merged Variantsdgv707n145
Supporting Variantsnssv14102549, nssv14100923, nssv14102175
Samplessample379, sample78, sample398
Known GenesETS2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112905
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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