A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114416



Internal ID21297682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51640741..51641910hg38UCSC Ensembl
Innerchr17:49718102..49719271hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381170
hg191170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097762
Samplessample276
Known GenesCA10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114416
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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