A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116170



Internal ID21299436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163139554..163228010hg38UCSC Ensembl
Innerchr3:162857342..162945798hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3888457
hg1988457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv819n145
Supporting Variantsnssv14108631
Samplessample370
Known GenesCT64
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116170
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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