A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154551



Internal ID22085056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11901648..11993394hg38UCSC Ensembl
Outerchr10:11897482..11996036hg38UCSC Ensembl
Innerchr10:11943647..12035393hg19UCSC Ensembl
Outerchr10:11939481..12038035hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3898555
hg1998555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004588
Samples
Known GenesUPF2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154551
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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