A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394108



Internal ID21051661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88904670..89082291hg38UCSC Ensembl
chr4:89825821..90003442hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38177622
hg19177622
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214777
Samples
Known GenesFAM13A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394108
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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