A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539093



Internal ID20912400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20723286..20724015hg38UCSC Ensembl
chr22:21077574..21078303hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072964
Samples
Known GenesPI4KA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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