A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758809



Internal ID20534669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1987637..1987637hg38UCSC Ensembl
chr4:1989364..1989364hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276270
Samples
Known GenesNELFA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758809
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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