A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449276



Internal ID21106829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107360034..107371418hg38UCSC Ensembl
chr9:110122315..110133699hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3811385
hg1911385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449276
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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