A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110504



Internal ID21293770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8788743..8801123hg38UCSC Ensembl
Innerchr9:8788743..8801123hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3812381
hg1912381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089454
Samplessample37
Known GenesPTPRD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110504
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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