A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154647



Internal ID22085152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100595356..100602358hg38UCSC Ensembl
Outerchr10:100593584..100604247hg38UCSC Ensembl
Innerchr10:102355113..102362115hg19UCSC Ensembl
Outerchr10:102353341..102364004hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3810664
hg1910664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006078
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154647
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer