A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113218



Internal ID21296484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:74863599..74867621hg38UCSC Ensembl
Innerchr5:74159424..74163446hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg384023
hg194023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108447
Samplessample149
Known GenesFAM169A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113218
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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