A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450254



Internal ID21107807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33042501..33047100hg38UCSC Ensembl
chr9:33042499..33047098hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230867
Samples
Known GenesSMU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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