A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535853



Internal ID20909207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17754868..17755188hg38UCSC Ensembl
chr22:18237634..18237954hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072854
Samples
Known GenesBID
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535853
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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