A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075053



Internal ID20642093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47600393..47614188hg38UCSC Ensembl
chr22:47996142..48009937hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3813796
hg1913796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075053
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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