A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073778



Internal ID20640818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32356627..32360175hg38UCSC Ensembl
chr22:32752614..32756162hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg383549
hg193549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554740
Supporting Variants
Samples
Known GenesRFPL3, RFPL3S
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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