A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154554



Internal ID22085059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14943303..15024489hg38UCSC Ensembl
Outerchr10:14942090..15028146hg38UCSC Ensembl
Innerchr10:14985302..15066488hg19UCSC Ensembl
Outerchr10:14984089..15070145hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3886057
hg1986057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004592
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154554
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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