A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114609



Internal ID21297875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4511170..4522040hg38UCSC Ensembl
Innerchr10:4553362..4564232hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3810871
hg1910871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089066
Samplessample81
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114609
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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