A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073498



Internal ID21982731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92034776..92034776hg38UCSC Ensembl
chr8:93047004..93047004hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584871
Samples
Known GenesRUNX1T1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073498
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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