A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154639



Internal ID22085144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87237542..87353136hg38UCSC Ensembl
Outerchr10:87216840..87357543hg38UCSC Ensembl
Innerchr10:88997299..89112893hg19UCSC Ensembl
Outerchr10:88976597..89117300hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38140704
hg19140704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv38n97
Supporting Variantsnssv4006063, nssv4006062
Samples
Known GenesLOC439994, NUTM2A, NUTM2A-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154639
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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