A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068827



Internal ID21978060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98220797..98220797hg38UCSC Ensembl
chr8:99233025..99233025hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585506
Samples
Known GenesNIPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068827
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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