A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433937



Internal ID21395939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:166880213..166909212hg38UCSC Ensembl
chr3:166598001..166627000hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3829000
hg1929000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15751347, nssv15752503
SamplesNB08, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433937
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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