A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431392



Internal ID21393394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80655245..80659244hg38UCSC Ensembl
chr10:82415001..82419000hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748831
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431392
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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