A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113286



Internal ID21296552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19866890..19868826hg38UCSC Ensembl
Innerchr17:19770203..19772139hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381937
hg191937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv484n145
Supporting Variantsnssv14098581
Samplessample361
Known GenesULK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113286
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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