A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438064



Internal ID21095617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98098698..98121810hg38UCSC Ensembl
chr9:100860980..100884092hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3823113
hg1923113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183171
Samples
Known GenesCORO2A, TRIM14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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