A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108511



Internal ID21283681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149968878..149972216hg38UCSC Ensembl
Innerchr3:149686665..149690003hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg383339
hg193339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113729
Supporting Variants
Samplessample348
Known GenesLOC646903, PFN2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108511
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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