A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765661



Internal ID20541521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43947983..43947983hg38UCSC Ensembl
chr4:43950000..43950000hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765661
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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