A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390726



Internal ID21381861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142824177..142824243hg38UCSC Ensembl
chr3:142543019..142543085hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15707243
Samples
Known GenesPCOLCE2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390726
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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