A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550765



Internal ID20923905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21850251..21855713hg38UCSC Ensembl
chr22:22204540..22210002hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg385463
hg195463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072614
Samples
Known GenesMAPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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