A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113744



Internal ID21297010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:88325038..88331986hg38UCSC Ensembl
Innerchr5:87620855..87627803hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg386949
hg196949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108888
Samplessample184
Known GenesTMEM161B-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113744
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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