A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538713



Internal ID20912027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17661343..17670617hg38UCSC Ensembl
chr22:18144109..18153383hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg389275
hg199275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071614
Samples
Known GenesBCL2L13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538713
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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