A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114786



Internal ID21298052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32346002..32349468hg38UCSC Ensembl
Innerchr10:32634930..32638396hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383467
hg193467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090152
Samplessample138
Known GenesEPC1, LOC102031319
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114786
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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