A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073966



Internal ID20641006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38418594..38422184hg38UCSC Ensembl
chr22:38814599..38818189hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383591
hg193591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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