A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110633



Internal ID21293899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27605141..27610592hg38UCSC Ensembl
Innerchr15:27850287..27855738hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg385452
hg195452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097143, nssv14096002
Samplessample323, sample55
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110633
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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