A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454950



Internal ID21112503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93714268..93719214hg38UCSC Ensembl
chr9:96476550..96481496hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384947
hg194947
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454950
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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