A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110444



Internal ID21293710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:30664777..30670053hg38UCSC Ensembl
Innerchr8:30522294..30527570hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385277
hg195277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087203
Samplessample140
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110444
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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