A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116210



Internal ID21299476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95856674..95926529hg38UCSC Ensembl
Innerchr13:96508928..96578783hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3869856
hg1969856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095653
Samplessample174
Known GenesUGGT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116210
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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