A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554579



Internal ID20927672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19143153..19143730hg38UCSC Ensembl
chr22:19130666..19131243hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072886
Samples
Known GenesDGCR14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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