A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070866



Internal ID21980099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138692270..138692270hg38UCSC Ensembl
chr8:139704513..139704513hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589876
Samples
Known GenesCOL22A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070866
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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