A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154646



Internal ID22085151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98075189..98077645hg38UCSC Ensembl
Outerchr10:98075083..98085972hg38UCSC Ensembl
Innerchr10:99834946..99837402hg19UCSC Ensembl
Outerchr10:99834840..99845729hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3810890
hg1910890
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006077, nssv4006076, nssv4006075
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154646
Frequency
Sample Size131
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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