A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154662



Internal ID22085167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123678943..123687597hg38UCSC Ensembl
Outerchr10:123678204..123689229hg38UCSC Ensembl
Innerchr10:125438459..125447113hg19UCSC Ensembl
Outerchr10:125437720..125448745hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3811026
hg1911026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005518
Samples
Known GenesGPR26
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154662
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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