A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071614



Internal ID20638654
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 StatusS
Merged Variantsnsv6538713
Supporting Variants
Samples
Known GenesBCL2L13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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