A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453908



Internal ID21111461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90413001..90415300hg38UCSC Ensembl
chr9:93175283..93177582hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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