A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055425



Internal ID21964658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:232897811..232897811hg38UCSC Ensembl
chr2:233762521..233762521hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536414
Samples
Known GenesNGEF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055425
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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