A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074568



Internal ID20641608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42370938..42371759hg38UCSC Ensembl
chr22:42766944..42767765hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552974
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074568
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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