A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390348



Internal ID21381483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12428891..12428964hg38UCSC Ensembl
chr3:12470390..12470463hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15707034
Samples
Known GenesPPARG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390348
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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