A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154659



Internal ID22085164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122572780..122598210hg38UCSC Ensembl
Outerchr10:122564250..122623497hg38UCSC Ensembl
Innerchr10:124332296..124357726hg19UCSC Ensembl
Outerchr10:124323766..124383013hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3859248
hg1959248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004530
Samples
Known GenesDMBT1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154659
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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