A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154610



Internal ID22085115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59586408..59653487hg38UCSC Ensembl
Outerchr10:59582233..59656438hg38UCSC Ensembl
Innerchr10:61346166..61413245hg19UCSC Ensembl
Outerchr10:61341991..61416196hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3874206
hg1974206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005785, nssv4005784, nssv4005783
Samples
Known GenesSLC16A9
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154610
Frequency
Sample Size131
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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