A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154606



Internal ID22085111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56797311..56894394hg38UCSC Ensembl
Outerchr10:56792858..56895120hg38UCSC Ensembl
Innerchr10:58557071..58654154hg19UCSC Ensembl
Outerchr10:58552618..58654880hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38102263
hg19102263
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004819
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154606
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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