A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106478



Internal ID21270627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189647214..189653058hg38UCSC Ensembl
Innerchr3:189365003..189370847hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg385845
hg195845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113862
Supporting Variants
Samplessample153
Known GenesTP63
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106478
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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