A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433724



Internal ID21395726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240308584..240310583hg38UCSC Ensembl
chr2:241248001..241250000hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754476
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433724
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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