A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051426



Internal ID21960659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100104807..100104807hg38UCSC Ensembl
chr2:100721269..100721269hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534289
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051426
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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