A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454943



Internal ID21112496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117261228..117284451hg38UCSC Ensembl
chr9:120023507..120046730hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3823224
hg1923224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230633
Samples
Known GenesASTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454943
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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