A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073566



Internal ID20640606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32852005..32872737hg38UCSC Ensembl
chr22:33247992..33268724hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3820733
hg1920733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537097
Supporting Variants
Samples
Known GenesSYN3, TIMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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