A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450925



Internal ID21108478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99905401..99907300hg38UCSC Ensembl
chr9:102667683..102669582hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233941
Samples
Known GenesLOC441461, STX17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450925
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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