A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070074



Internal ID21979307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142255935..142255935hg38UCSC Ensembl
chr8:143337296..143337296hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586091
Samples
Known GenesTSNARE1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070074
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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