A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554360



Internal ID20927462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35580831..35586849hg38UCSC Ensembl
chr22:35976878..35982896hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg386019
hg196019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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