A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111807



Internal ID21295073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:82657316..82659010hg38UCSC Ensembl
Innerchr5:81953135..81954829hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg381695
hg191695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv979n145
Supporting Variantsnssv14108406, nssv14109292, nssv14097415, nssv14108846, nssv14109070, nssv14109332
Samplessample312, sample140, sample300, sample111, sample231, sample172
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111807
Frequency
Sample Size467
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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