A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106372



Internal ID21269313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183252088..183255003hg38UCSC Ensembl
Innerchr3:182969876..182972791hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg382916
hg192916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111029
Supporting Variants
Samplessample138
Known GenesB3GNT5, MCF2L2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106372
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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