A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433946



Internal ID21395948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171502212..171504211hg38UCSC Ensembl
chr3:171220001..171222000hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753517
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433946
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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