A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114801



Internal ID21298067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130660375..130666304hg38UCSC Ensembl
Innerchr9:133535762..133541691hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg385930
hg195930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088171
Samplessample373
Known GenesPRDM12
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114801
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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