A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116136



Internal ID21299402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:70701618..70734913hg38UCSC Ensembl
Innerchr8:71613853..71647148hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3833296
hg1933296
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086247
Samplessample262
Known GenesXKR9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116136
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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