A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454772



Internal ID21112325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41277801..41364700hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3886900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7732n223
Supporting Variantsnssv18221359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454772
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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