A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111769



Internal ID21295035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:49359688..49364575hg38UCSC Ensembl
Innerchr17:47437050..47441937hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg384888
hg194888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097656
Samplessample216
Known GenesZNF652
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111769
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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