A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442959



Internal ID21100512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130239322..130248621hg38UCSC Ensembl
chr9:133001601..133010900hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442959
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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