A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111708



Internal ID21294974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:48553940..48557802hg38UCSC Ensembl
Innerchr8:49466500..49470362hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg383863
hg193863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086236
Samplessample259
Known GenesLOC101929268
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111708
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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