A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117257



Internal ID21300523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189647426..189653058hg38UCSC Ensembl
Innerchr3:189365215..189370847hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg385633
hg195633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv836n145
Supporting Variantsnssv14105461
Samplessample394
Known GenesTP63
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117257
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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