A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116360



Internal ID21299626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55203511..55209364hg38UCSC Ensembl
Innerchr8:56116071..56121924hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg385854
hg195854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1183n145
Supporting Variantsnssv14086024, nssv14086239
Samplessample198, sample259
Known GenesXKR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116360
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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