A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111578



Internal ID21294844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129691489..129701323hg38UCSC Ensembl
Innerchr9:132453768..132463602hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg389835
hg199835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088475
Samplessample33
Known GenesPRRX2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111578
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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