A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051453



Internal ID21960686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235764766..235764766hg38UCSC Ensembl
chr2:236673410..236673410hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528335
Samples
Known GenesAGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051453
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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