A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753440



Internal ID20529300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165920766..165920766hg38UCSC Ensembl
chr2:166777276..166777276hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292427
Samples
Known GenesTTC21B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753440
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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