A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753006



Internal ID20528866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42221962..42221962hg38UCSC Ensembl
chr1:42687633..42687633hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278716
Samples
Known GenesFOXJ3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753006
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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