A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553072



Internal ID20926187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19550063..19551570hg38UCSC Ensembl
chr22:19537586..19539093hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381508
hg191508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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