A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106399



Internal ID21269748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:88658829..88665783hg38UCSC Ensembl
Innerchr3:88707979..88714933hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg386955
hg196955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112665
Supporting Variants
Samplessample142
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106399
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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