A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207520



Internal ID20774560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42780866..42782448hg38UCSC Ensembl
chr22:43176872..43178454hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg381583
hg191583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540455
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207520
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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