A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154597



Internal ID22085102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49357759..49387884hg38UCSC Ensembl
Outerchr10:49356586..49401267hg38UCSC Ensembl
Innerchr10:50565804..50595930hg19UCSC Ensembl
Outerchr10:50564631..50609313hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3844682
hg1944683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004755
Samples
Known GenesDRGX
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154597
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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