A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117157



Internal ID21300423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:81755341..81759026hg38UCSC Ensembl
Innerchr5:81051160..81054845hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg383686
hg193686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097456
Samplessample124
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117157
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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