A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110923



Internal ID21294189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:107646795..107651627hg38UCSC Ensembl
Innerchr10:109406553..109411385hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg384833
hg194833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089029
Samplessample60
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110923
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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