A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550902



Internal ID20924044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26683639..26685476hg38UCSC Ensembl
chr22:27079602..27081439hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381838
hg191838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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