A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428022



Internal ID21085575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138691317..138717326hg38UCSC Ensembl
chr8:139703560..139729569hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3826010
hg1926010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223543
Samples
Known GenesCOL22A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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