A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111049



Internal ID21294315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24084914..24122334hg38UCSC Ensembl
Innerchr3:24126405..24163825hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3837421
hg1937421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108624, nssv14108724
Samplessample369, sample387
Known GenesLINC00691, THRB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111049
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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