A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117582



Internal ID21300848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22143179..22424525hg38UCSC Ensembl
Innerchr17:21669785..21923854hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38281347
hg19254070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097626
Samplessample206
Known GenesFAM27L, FLJ36000
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117582
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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