A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112213



Internal ID21295479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19865283..19868888hg38UCSC Ensembl
Innerchr17:19768596..19772201hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383606
hg193606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv483n145
Supporting Variantsnssv14098877
Samplessample138
Known GenesULK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112213
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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