A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049050



Internal ID21958283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:232575276..232575276hg38UCSC Ensembl
chr2:233439986..233439986hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535215
Samples
Known GenesEIF4E2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049050
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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