A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106713



Internal ID21273563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176111688..176185169hg38UCSC Ensembl
Innerchr3:175829476..175902957hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3873482
hg1973482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113092
Supporting Variants
Samplessample192
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106713
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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