A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111150



Internal ID21294416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145383027..145384907hg38UCSC Ensembl
Innerchr6:145704163..145706043hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087728, nssv14086308, nssv14089221, nssv14083780, nssv14084467
Samplessample82, sample223, sample95, sample118, sample287
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111150
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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