A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765643



Internal ID20541503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104421918..104421918hg38UCSC Ensembl
chr2:105038376..105038376hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267577
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765643
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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