A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426620



Internal ID21084173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19375227..19474328hg38UCSC Ensembl
chr9:19375225..19474326hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3899102
hg1999102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7639n223
Supporting Variantsnssv18221577
Samples
Known GenesACER2, RPS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426620
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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