A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118153



Internal ID21301419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248595051..248627699hg38UCSC Ensembl
Innerchr1:248758352..248791000hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3832649
hg1932649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv134n145
Supporting Variantsnssv14091441
Samplessample289
Known GenesOR2T11
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118153
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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