A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047245



Internal ID21956478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99082099..99082099hg38UCSC Ensembl
chr2:99698562..99698562hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523508
Samples
Known GenesTSGA10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047245
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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