A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113696



Internal ID21296962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25526331..25529871hg38UCSC Ensembl
Innerchr12:25679265..25682805hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg383541
hg193541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093780
Samplessample362
Known GenesIFLTD1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113696
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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