A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117616



Internal ID21300882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36160540..36172705hg38UCSC Ensembl
Innerchr3:36202032..36214197hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3812166
hg1912166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105396
Samplessample114
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117616
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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