A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154571



Internal ID22085076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32167619..32211397hg38UCSC Ensembl
Outerchr10:32165341..32218336hg38UCSC Ensembl
Innerchr10:32456547..32500325hg19UCSC Ensembl
Outerchr10:32454269..32507264hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3852996
hg1952996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004706
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154571
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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