A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553045



Internal ID20926160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11818901..11900600hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3881700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553045
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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