A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154555



Internal ID22085060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18577939..18650553hg38UCSC Ensembl
Outerchr10:18576029..18655757hg38UCSC Ensembl
Innerchr10:18866868..18939482hg19UCSC Ensembl
Outerchr10:18864958..18944686hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3879729
hg1979729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004593
Samples
Known GenesNSUN6
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154555
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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