A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112931



Internal ID21296197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4227953..4239611hg38UCSC Ensembl
Innerchr10:4270145..4281803hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3811659
hg1911659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088651, nssv14088699
Samplessample242, sample270
Known GenesLINC00702
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112931
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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