A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019850



Internal ID21929193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100421053..100435461hg38UCSC Ensembl
chr9:103183335..103197743hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3814409
hg1914409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589899
Samples
Known GenesMSANTD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019850
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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